Economic Review
Global Economic Review
The global economy demonstrated resilience in 2024, navigating a complex environment marked by geopolitical tensions, widespread elections across more than 60 countries, including five major economies and evolving monetary policies. Despite these uncertainties, global output grew by 3.3%, staying above recession thresholds but below prepandemic trends.
Inflation began to ease, supported by tighter monetary policy and cooling labour markets. Real household incomes improved due to falling inflation and steady wage growth, although consumer confidence remained fragile. Interest rates saw a shift during the year, with central banks in both advanced and developing economies initiating rate cuts to support growth as inflation moderated.
Global merchandise trade also rebounded, expanding 2.9%, its strongest performance relative to GDP since 2017. However, growth remained uneven, with strength in India and the US, a slowdown in China, and weak momentum in the Eurozone. Geopolitical conflicts continued to disrupt energy flows and supply chains, underscoring persistent systemic vulnerabilities.
Geopolitical Conflicts and U.S. Tariff Actions
The global economic environment in 2025 remains challenged by a combination of ongoing geopolitical conflicts and trade tensions. Prolonged conflicts in Ukraine and the Middle East continue to disrupt global supply chains, particularly in energy and key commodities, while emerging flashpoints in Asia and Africa add further complexity to the operating environment.
In parallel, recent tariff announcements by the United States have introduced additional uncertainty for global trade flows and investment decisions. These policy shifts have contributed to a moderation in U.S. growth forecasts and are weighing on global business sentiment. Companies are increasingly cautious, with several delaying capital deployment amid policy unpredictability.
The combined impact of geopolitical instability and protectionist measures is likely to influence global inflation trends, supply chain realignments, and capital flows in the near to medium term. Businesses are expected to remain focused on risk mitigation, diversification, and supply resilience as these factors evolve.
Looking ahead to 2025 and 2026, the global economy faces a cautiously optimistic but uneven path. According to the IMF, global growth is projected at 2.8% in 2025 and 3.0% in 2026. Advanced economies are expected to grow more slowly, while emerging markets may face varying recovery trajectories, reflecting the divergence in growth path.
Inflation is forecast to decline to 4.2% in 2025 and 3.5% in 2026, with advanced economies likely
to reach targets sooner than emerging markets. Central banks are expected to continue adjusting their policies cautiously, balancing growth support with inflation control.
Additionally, the global push for sustainability and the energy transition is influencing capital flows and industrial policy, with many economies aligning public investment and regulatory frameworks towards low-carbon growth. Also, the adoption of AI andautomation is expected to drive incremental productivity gains, supporting longterm competitiveness and economic resilience.
While downside risks remain, from geopolitical volatility to supply chain pressures, the global economy is broadly positioned for a period of gradual recovery, supported by easing inflation, renewed consumer demand, and evolving growth strategies across regions. /
| Global Growth Forecast (%) | ||||
| Particulars | 2023* | 2024 | 2025 (P) | 2026 (P) |
| World Output | 3.2 | 3.3 | 2.8 | 3.0 |
| Advanced Economies | 1.6 | 1.8 | 1.4 | 1.5 |
| US | 2.5 | 2.8 | 1.8 | 1.7 |
| Eurozone | 0.4 | 0.9 | 0.8 | 1.2 |
| Japan | 1.9 | 0.1 | 0.6 | 0.6 |
| UK | 0.1 | 1.1 | 1.1 | 1.4 |
| Other Advanced Economies | 1.8 | 2.2 | 1.8 | 2.0 |
| Emerging Market and Developing Economies | 4.3 | 4.3 | 3.7 | 3.9 |
| China | 5.2 | 5.0 | 4.0 | 4.0 |
| India | 7.8 | 6.5 | 6.2 | 6.3 |
| Emerging Market and Middle-Income Economies | 4.4 | 4.3 | 3.7 | 3.8 |
| Low-income Developing Countries | 4.0 | 4.0 | 4.2 | 5.2 |
Source: World Economic Outlook, IMF, April 2025 Note:
2
P stands for projections.2
For India, data and forecasts are presented on a fiscal year basis, with FY 2024/25 (starting in April 2024) shown in the 2024 column. Indias growth projections are 6.5% in 2025 and 6.2% in 2026 based on the calendar year.*Source: World Economic Outlook, IMF, April 2024
Indian Economic Review
India remained the fastest- growing major economy in 2024-25 and became the fourth- largest globally, with real GDP growth estimated at 6.5% by the National Statistical Office (NSO), moderating from 9.2% in the previous year. The slowdown was attributed to reduced government capital expenditure, sluggish private investment, and weak consumption demand.
Despite this moderation, the economy demonstrated resilience. Nominal GDP tripled over the past decade, reaching INR 331.03 trillion, supported by structural reforms, digitalisation, a stable banking system, and containing inflation. The Union Budget 2025-26 aimed to revive investment momentum through infrastructure spending, social welfare measures, and digital public infrastructure to stimulate domestic demand and promote inclusive growth.
Indias total exports rose 76% over the past decade, reaching USD 825 billion in 2024-25, led by engineering goods, electronics, and pharmaceuticals. The pharmaceutical sector strengthened its global position as the third-largest producer by volume, with exports to over 200 countries. Drug and pharmaceutical exports alone grew by 98% over the decade to USD 30.5 billion, driven by strong demand for generics, APIs, and formulations. The United States remained the largest destination, accounting for nearly a third of Indias pharma exports, followed by the European Union, UK, Brazil, and South Africa. Additionally, India achieved a record foodgrain production of 347 MT, with agri-exports accounting for
11.7% of total exports, driven by improved productivity and enabling policies.
Outlook
Indias economic outlook for 2025 and 2026 remains among the strongest globally, as reaffirmed by the NSO and RBI, even as other major economies face downward growth revisions. India is projected to grow at a stable 6.5% in 2025-26, supported by resilient domestic consumption, particularly in rural areas, rising public and private investment, expanding FDI, and greater integration into global trade and supply chains. According to the NSO, growth will also be underpinned by sustained momentum in infrastructure development, a strong services sector, and steady performance in manufacturing and construction. Improving export competitiveness and a stable macroeconomic environment further reinforce Indias position as one of the worlds fastest- growing major economies.
The Union Budget 2025-26 introduced significant tax relief to boost consumer spending raising the tax free income V
threshold to INR 12 Lakh (effective exemption up to INR 12.75 Lakh, including standard deduction), expanding rebates and deductions to increase disposable income for middle income and rural households. Concurrently, the RBI implemented a larger- than-expected 50 bps repo rate reduction, cutting the policy rate from 6.0% to 5.5%, alongside a 100 bps CRR cut, to ease lending costs and stimulate demand.
This outlook is supported by solid macroeconomic fundamentals and a wide- ranging reform agenda spanning infrastructure, innovation, and financial inclusion. Flagship programmes like Make in India and the National Infrastructure Pipeline are accelerating industrial development, while the digital economy continues to boost productivity and expand access.
Indias appeal as an investment destination is further enhanced by improved ease of doing business, proactive economic diplomacy, and strategic global partnerships.
The pharmaceutical sector is also emerging as a key growth driver, with the market projected to reach USD 130 billion by 2030, supported by rising healthcare demand and growing R&D investment.
While challenges such as geopolitical tensions, oil price volatility, rural distress, and climate-related disruptions remain, sustained policy discipline and ongoing structural reforms, particularly in governance, regulatory simplification, and labour flexibility, will be critical for long-term growth.
With its resilient economic base and clear strategic focus, India is well-positioned to sustain its trajectory and move toward its goal of becoming a developed economy by 2047.
J
Indias Growth Forecast (%) |
||||
Perticulars |
2022-23 | 2023-24 | 2024-25 (E) | 2025-26 (P) |
Indias Growth Forecast |
7.6 | 9.2 | 6.5 | 6.5 |
Industry and Business Review
Global Pharmaceutical Industry
The global pharmaceutical industry is undergoing a period of steady transformation, shaped by scientific innovation, demographic shifts, the rising prevalence of chronic diseases, and increasing digital adoption. In 2024, the global pharmaceutical market was valued at USD 1,654 billion and is projected to grow from USD 1,746 billion in 2025 to USD 3,529 billion by 2035, reflecting a CAGR of 6.49% over the forecast period (2025-2035). While mature markets such as North America, Western Europe, and Japan are expected to grow at a slower pace due to already high per capita consumption, emerging economies like India, China, Southeast Asia, and Latin America are set to drive the next phase of volume-led growth. Asia Pacific, in particular, is projected to be the fastest-growing region during this period.
Multiple structural drivers are supporting this growth trajectory. These include an ageing global population, increasing incidence of chronic conditions, expanding healthcare spending
by governments, and ongoing efforts to make medicines more accessible and affordable. Rising awareness and diagnosis rates in underserved regions, along with the introduction of low-cost OTC medications, are further contributing to global demand.
Therapeutic innovation remains a key growth driver, particularly in oncology and immunology, followed by mental health.
The growing use of specialty medicines, along with the adoption of advanced biologics and small molecule therapies, continues to shape treatment patterns. A notable shift is being seen in metabolic care with the rapid uptake of GLP-1 drugs for diabetes and obesity, which are expected to significantly influence future usage trends. Fuelled by new brands and sustained investment in high-value therapies, overall spending remains robust across regions, despite pricing pressures and increasing reliance on confidential rebates in many markets.
Digital transformation is becoming integral to the industrys evolution. Pharmaceutical companies are increasingly leveraging AI, real- world evidence, and digital health platforms to streamline clinical trials, improve patient targeting, and optimise treatment delivery. These technologies are enhancing productivity, improving outcomes, and enabling faster response to patient needs.
At the same time, access and affordability remain ongoing challenges. High-income countries continue to consume twice as more medicines than low-income regions, where gaps in infrastructure, affordability, and distribution persist. In response, many healthcare systems, especially in developed markets, are adopting value-based pricing models, encouraging the use of generics and biosimilars, and exploring alternative reimbursement mechanisms to balance innovation with sustainability.
| Global Pharmaceutical Market | (USD Billion) | |||
| Regions | 2024 | 2020-2024 CAGR | 2029 | 2025-2029 CAGR |
| Developed Markets | 1,421.5 | 8.2% | 1,945-1,975 | 5.5-8.5% |
| Pharmerging Markets | 312.2 | 6.0% | 375-405 | 3.5-6.5% |
| Other Markets | 16.1 | 1.0% | 18-22 | 2-5% |
| Global Pharmaceutical Market | 1,749.8 | 7.7% | 2,355-2,385 | 5-8% |
Source: IQVIA 2025 report
Global Pharmaceutical Market - Share by Product Type
Region |
Original Brands |
Non-original Brands |
Unbranded Generics |
OTC, Vaccines and Others |
Total |
|||||
Year |
2024 | 2029 | 2024 | 2029 | 2024 | 2029 | 2024 | 2029 | 2024 | 2029 |
Developed Markets |
1,091.6 | 1,555 1,585 | 120.6 | 135-165 | 124.6 | 120-150 | 84.7 | 95-115 | 1,421.5 | 1,945-1,975 |
Pharmerging Markets |
88.4 | 115-135 | 106.3 | 120-140 | 41.1 | 40-60 | 76.5 | 80-100 | 312.2 | 375-405 |
Other Markets |
4.4 | 3-7 | 8.4 | 8-12 | 0.8 | 0.7-1.1 | 2.6 | 2.5-3.5 | 16.1 | 18-22 |
Global Markets |
1,184.3 | 1,685- | 235.3 | 270-300 | 166.5 170-200 |
163.7 | 180-210 | 1,749.8 | 2,355-2,385 | |
Developed Markets
Medicine spending in developed markets is expected to reach USD 1,945 to USD 1,975 billion by 2029, driven by new and innovative treatments, even as generics and biosimilars increase competition. Immunology drugs are seeing steady use, with nearly half now facing biosimilar competition that is boosting access. Over time, spending is set to rise further, supported by medicines from established brands and new product launches.
| Developed Markets - | Pharmaceutical Spending and Growth | (USD Billion) | ||
| Region/Country | 2024 | 2020-2024 CAGR | 2029 | 2025-2029 CAGR |
| Top 10 Developed Markets | 1,194.5 | 8.2% | 1,635-1,665 | 5-8% |
| Other Developed Markets | 227.0 | 7.8% | 295-325 | 5.5-8.5% |
| Total Developed Markets | 1,421.5 | 8.2% | 1,945-1,975 | 5.5-8.5% |
Growth by Region
The global pharmaceutical market is expanding across all major regions, with spending projected to grow by over 30% in North America, Europe, Asia Pacific, Latin America, and the Middle East & Africa. This growth is being driven by population expansion, rising healthcare needs, and increased use of high- value therapies.
North America, holding 41.87% of the global market share in 2024, is led by the U.S., where high healthcare spending, strong policies, and robust biopharma investments fuel demand for
biologics, oncology, and rare disease treatments. Hospital pharmacies dominate, with retail and online channels growing in chronic care.
In Europe, steady growth is supported by strong regulation and funding. Germany, France, and the UK lead the region, driven by demand for chronic and specialty treatments, biologics, and biosimilars.
Asia Pacific is the fastest-growing region, led by China, India, and Japan, backed by local manufacturing, growing clinical research, and broader healthcare
access. China, the second-largest market, is set to grow volume by 8% and spending by 15% over five years, driven by access to novel drugs via the NRDL. Japan benefits from government support and demand for ageing and metabolic care.
In Latin America, the Middle East and Africa, growth is moderate and led by government initiatives, local production, and demand for chronic and infectious disease treatments, and are expanding through healthcare reforms and biopharma investments.
Megatrends
Personalised Medicine = and Genomics
The rise of genomic data has enabled the advancement of personalised medicine. Pharmaceutical companies are leveraging genetic insights to create therapies tailored to individual patient profiles. This approach not only enhances treatment effectiveness but also helps minimise adverse side effects
Biotechnology remains a key driver of innovation in drug development. Emerging biological therapies, including gene and cell therapies, are opening up new possibilities for treating conditions that have historically been difficult to manage.
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Digital Health and TelemedicineDigital technologies and telemedicine are transforming healthcare delivery, allowing patients to access medical advice and treatment remotely. Pharmaceutical companies are increasingly investing in digital health tools that support better patient outcomes and improve treatment adherence, particularly benefitting underserved and rural communities.
U.S. Food and Drug Administrations (FDA) Drug Approvals
In 2024, the FDAs Centre for Drug Evaluation and Research (CDER) approved 50 novel drugs never before marketed in the U.S., including gene therapies, RNA-based treatments, and CAR-T cell therapies, highlighting the agencys focus on precision medicine and expanding treatment options for previously untreatable conditions. FDA approvals are projected to increase to 70 in 2025, reflecting a sustained pipeline of innovation.
Between 2014 and 2023, the FDA approved 176 new drugs for the top 20 pharmaceutical companies, along with 33 postapproval acquisitions and 83 first- in-class launches, the majority in oncology. The U.S. remains the dominant first-launch market, with 40% of U.S.-launched NAS over the past five years still pending in key European marketsunderscoring global access lags. Conversely, only 7% of Europe-launched drugs were not introduced in the U.S.
Regulatory complexity, along with evolving reimbursement and patent frameworks, continues to shape both innovation and accessibility, particularly in emerging economies.
New Drug Launches
The global drug development pipeline remains robust, with over 20,000 active programmes underway, 17% in Phase 1,
16% in Phase 2, and 6% in Phase 3. Among these, 69 New Active Substances (NAS) are in late-stage development, with oncology and immunology leading to therapeutic focus. Roughly 20% of late- stage pipelines of the top 20 pharmaceutical companies signal strong near-term commercial potential.
A notable shift is the increasing role of emerging biopharma (EBP) companies in bringing innovation to the market. In 2024 85% of the 48 NAS launches originated from EBPs, with 41 of those launched directly by the originating company. Between 2020 and 2024, EBPs accounted for 59% of all NAS launches, marking a steady rise in their contribution to
the global pipeline. EBPs are now progressing more assets through late-stage development, reflecting a reduced dependency on licensing to larger firms.
Globally, new drugs do not launch uniformly. The U.S. remains the most frequent first-launch country, while other markets often face delays of a year or more due to regulatory review cycles, pricing negotiations, and reimbursement hurdles. These delays contribute to ongoing disparities in timely access to novel therapies across geographies, especially between developed and emerging markets.
Pharmaceutical R&D
Pharmaceutical R&D remains central to industry growth, with global spending exceeding USD 244 billion in 2023, including over USD 80 billion by U.S. companies alone. Driven by ageing populations, chronic diseases, and patent expirations, firms continue investing heavily in new therapies, particularly in oncology, immunology, and rare diseases.
The global pipeline includes over 20,000 active drug programmes, supported by rising biopharma funding, stabilised clinical trial volumes, and improved Phase III success rates. Companies are increasingly using AI, real-world evidence, and outsourcing to speed up development and reduce costs.
Trial cycle times have stabilised in 2024, with inter-trial intervals improving significantly from pandemic highs. Drugs like semaglutide, adalimumab, and apixaban led spending in
2023, reflecting strong market uptake of high-impact therapies. Strategic initiatives, such as the USD 14 Million investment in
the U.S. API Innovation Centre, highlight efforts to boost domestic capabilities and reduce supply chain dependence.
Indian Pharmaceutical Industry
Indias pharmaceutical market is expected to grow to USD 38-42 billion by 2028, with a CAGR of 7-10% from 2024, driven by rising healthcare access, strong demand for acute and chronic therapies, and a robust generics ecosystem. The sector ranks 3rd globally by volume and 14th by value, contributing 20% of the worlds generics and a large share of global vaccine supplies.
Affordable healthcare is becoming a national reality, with initiatives like PMBJPs 15,000+ Jan Aushadhi Kendras offering medicines at up to 80% lower prices. Production
Linked Incentive (PLI) schemes are spurring domestic manufacturing of APIs, critical drugs, and medical devices, while bulk drug parks and upgraded labs are cutting costs and boosting self-reliance.
The industrys turnover crossed INR 4.17 Trillion in 2023-24, growing steadily at over 10% annually. With PLI-backed projects, improved insurance coverage, foreign investments of INR 12,800+ Crore, and widespread job creation, Indias pharma sector is expanding and transforming lives at home and globally.
Global Active Pharmaceutical Ingredients (API) Industry
The global Active Pharmaceutical Ingredient (API) market is expanding steadily, projected to grow from over USD 260 billion in 2025 to more than USD 400 billion by 2030. Growth is driven by rising demand for generics, complex therapies, biologics, and
biosimilars, alongside increasing chronic disease prevalence and patent expirations. Technological innovation, regulatory tightening, and supply chain localisation are reshaping the landscape.
Regionally, North America leads in innovation and biologics.
Asia-Pacific, driven by India and China, dominates in volume and cost efficiency. Europe is focused on reshoring and quality. Latin America and MEA are seeing steady growth through rising healthcare needs and policy support.
Megatrends
Rise of Biologics and =
Specialty APIs
There is growing global demand for complex APIs used in targeted therapies, such as cancer immunotherapies and autoimmune drugs. Biologics and biosimilars are at the forefront of this trend, necessitating specialised infrastructure and advanced manufacturing techniques. This shift is reshaping the competitive landscape and pushing API players to invest in cell culture, recombinant technology, and monoclonal antibody production.
= Onshoring and Supply Chain Diversification
The COVID-19 pandemic exposed the vulnerabilities of global API supply chains.
In response, pharmaceutical companies and governments are localising manufacturing to reduce dependence on concentrated regions like China. This is leading to increased investments in domestic production hubs across the U.S., Europe, and India, and fostering API parks, PLI schemes, and regulatory fast-tracking.
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Green Chemistry and Sustainable ManufacturingEnvironmental concerns and tightening regulatory norms are accelerating the adoption of green chemistry principles in API production. Manufacturers are investing in technologies that reduce solvent usage, enable energy efficiency, and minimise hazardous waste, aligning with ESG goals and global sustainability commitments.
Indian Active Pharmaceutical Ingredients (API) Industry
Indias Active Pharmaceutical Ingredients (API) market is expected to grow from USD 13.64 billion in 2024 to USD 20.32 billion by 2029, at a CAGR of 8.31% (2024-2029), as per Mordor Intelligence.
In 2023-24 (April-January),
Indias drug and pharma exports reached USD 22.51 billion,
marking an 8.12% YoY growth. In January 2024 alone, exports stood at USD 2.13 billion, accounting for 5.8% of total exports.
To boost local manufacturing of key starting materials (KSMs) and APIs, the Indian government is promoting domestic production through its Production Linked Incentive (PLI) scheme.
India Active Pharmaceutical
Ingredients (API) Market
Market Size in USD Billion CAGR 8.31%
Global Contract Development and Manufacturing Organisation (CDMO) Industry
The global CDMO market is expected to grow at a CAGR of 7.2% from 2021 to 2026, driven by rising demand for specialised therapies and complex drugs.
As pharma companies focus on targeted treatments, they increasingly rely on CDMOs for development and large-scale manufacturing support. The growing biopharma sector also fuels demand for advanced capabilities, especially in biologics and novel formulations. CDMOs with cutting-edge technologies are becoming key partners, helping reduce costs and speed up drug launches.
The market spans two main service areas, contract development (covering drug discovery and pre-clinical work) and contract manufacturing (for commercial production). Pharmaceutical and biotech firms are the primary clients, leveraging CDMO expertise to streamline operations and gain flexibility.
Growth by Region
The U.S. CDMO market is expected to grow from USD 54.2 Billion in 2023 to USD 68.3 Billion by 2028, at a CAGR of 4.74%. Chinas CDMO market is set to expand from USD 27.1 Billion to USD 42.9 Billion over the same period, with a higher CAGR of 9.63%.
North America currently leads the global CDMO market due to its strong pharmaceutical and biotech industry and advanced clinical trial infrastructure. However, the Asia-Pacific region is expected to grow the fastest, driven by a rising domestic pharma market, skilled and affordable workforce, and government policies supporting CDMO growth.
iviyit ;vvu i.
Indian Contract Development and Manufacturing Organisation (CDMO) Industry
Indias CDMO industry is expanding rapidly, with market size estimated at USD 7.9 billion in 2024, projected to reach USD 15.4 billion by 2033, growing at a 7.7% CAGR from 2025 to 2033. Another forecast anticipates the market doubling to USD 14 billion by 2028, driven by cost advantages over China
and increasing demand from global pharma. Government support through PLI incentives and strong investments in biologics and tech platforms are accelerating this growth.
Although the proposed U.S. Biosecure Act has not been enacted, the underlying
concerns around supply chain security continue to influence global sourcing decisions. This trend presents an opportunity for Indian CDMOs to position themselves as reliable, compliant, and cost-effective partners as global pharma seeks to reduce dependency on China.
Megatrends
Biologics and Biosimilars ,==
Drive CDMO Investments
Indian CDMOs are rapidly expanding capabilities in biologics and biosimilars, including mammalian/microbial expression systems and single-use bioreactors. Rising global demand for affordable, high-quality immunotherapies and monoclonal antibodies is pushing India to become a preferred destination for biologics manufacturing. Regulatory alignment with U.S.
FDA and EMA is boosting trust and access to global markets.
=
Shift toward End-to- ==End Outsourcing
Pharma innovators increasingly prefer full-service CDMOs that can handle drug discovery, development, clinical trials, and commercial production. Indian CDMOs are responding by expanding into high-value areas like HPAPIs, sterile injectables, and complex generics. Tech integration, AI in drug discovery, automation, and real-time analytics, is improving speed, cost, and compliance.
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Strong Capex and Policy PushMajor investments (e.g.,
Aragens INR 2,000 Crore expansion) and PLI scheme support are accelerating infrastructure upgrades and capacity expansion. Government support, improved regulatory harmonisation, and global partnerships are positioning Indian CDMOs as strategic, long-term partners for pharmaceutical MNCs.
Hikal - Business Review of the Pharmaceutical Division
In 2024-25, our pharmaceutical business reported revenue of INR 11,681 Million and EBIT of INR 1,374 Million, marking a 47% y-o-y EBIT growth and a 327-bps margin improvement, driven by better capacity utilisation, operational efficiency, and a broader customer base.
Despite ongoing geopolitical uncertainty, supply chain realignments, and cost pressures, the global pharma industry remains resilient, and we see strong momentum heading into 2025-26. We are actively working to reduce supply chain risks through backward integration, alternate vendor development, and localisation initiatives, while continuing to drive operational efficiency and margin improvement.
Our API segment experienced notable volume growth during the year, driven by increased demand from both long-standing clients and newly acquired customers.
We continue to advance our portfolio expansion initiatives, which are beginning to yield
results as product registrations started to come through across multiple geographies. These developments position us well for accelerated growth in the near term. Meanwhile, our CDMO business remains a key growth driver, with strong RFP inflows from global innovators and specialty chemical players. We are capitalising on the global China+1 strategy, which is driving increased traction in CDMO engagements. Several projects are progressing through development and validation stages. Additionally, our food ingredients project is advancing well and marks a strategic diversification into high-value, adjacent segments.
We are strengthening our presence in complex, high- growth therapeutic areas and expanding into key international markets such as Japan, Latin America, Korea, the Middle East, and Southeast Asia. We are also focused on expanding our capabilities at the R&T site to drive future business and revenue growth. Our focus remains on product innovation, regulatory alignment, and
speed-to-market to build longterm customer relationships and ensure sustainable growth. We successfully cleared both the ANVISA GMP and PMDA audits at our Jigani facility, reinforcing our commitment to global quality standards.
In addition, we completed 22 customer audits during the financial year 2024-25, reflecting continued trust and confidence in our operations. We also made progress on our regulatory pipeline, with eight DMFs filed in 2024-25 and registrations secured in key regulated markets including the EU, Japan, and Australia.
We are also advancing our digital and Industry 4.0 initiatives across manufacturing and R&D. These efforts are driving operational agility, enhancing quality, and creating longterm differentiation.
Backed by these strengths, and with a strong pipeline of differentiated products, increased development activity, and a stable revenue mix in
2024- 25, we are well-positioned for a stronger performance in
2025- 26.
API
Hikals API divisions performance was led by strong volume growth, increased offtake of new molecules, and robust global contracts with major pharmaceutical companies.
The division remains focused on complex APIs and continues to expand its portfolio, supported
CDMO
Our Contract Development and Manufacturing Organisation (CDMO) segment remains a key growth engine. We have a strong pipeline of development projects from global pharma innovators and specialty chemical companies. Inquiry levels are rising across both early- and late-phase programmes, as customers seek reliable partners with high-quality development capabilities and
by sustained investments in R&D. With 8-9 differentiated products currently in the pipeline and plans to commercialise 2-3 new APIs annually, we are strengthening our position in high-growth and niche therapeutic areas. This strategy is also helping deepen our market presence across Japan,
backward-integrated supply chains. We have also enhanced our technology platforms and capabilities to handle the complex chemistries required by innovator customers.
During the year, we strengthened customer relationships in North America and Europe, as global supply chain diversification trends prompted partners to
Latin America, Korea, the Middle East, and Southeast Asia.
As part of our forward strategy, we will be investing in high- potency API (HPAPI) technology to serve the small-volume, high-value segment, marking a significant step into specialty and precision therapeutics.
seek more agile and dependable CDMO collaborators.
We saw an improved offtake from key clients, with several promising projects advancing toward development and validation stages. Additionally, our food ingredients project is progressing positively, reinforcing our diversification strategy and opening up new opportunities in high-value, adjacent sectors.
Global Animal Health Industry
According to Grand View Research, the global animal health market was valued at USD 62.89 billion in 2024 and is projected to reach USD 112.33 billion by 2030, growing at a CAGR of 10.46%. IMARC places it at USD 38.99 billion in 2024, expected to reach USD 51.33 billion by 2033, with a CAGR of 2.79%. North America led the market with a 44.9% share in 2024, driven by high pet ownership, quality veterinary care, and robust infrastructure.
Growth in the market is driven by rising concerns over zoonotic
infections, which have led to increased investments in vaccines, diagnostics, and antimicrobial therapies. Governments are tightening regulations and expanding disease surveillance, while public campaigns are promoting responsible pet ownership and vaccination. The livestock sector is strengthening biosecurity to prevent disease outbreaks and ensure food safety.
Advances in veterinary diagnostics enable faster detection and response to emerging threats.
Pharmaceutical companies are actively developing new therapies and biologics to combat zoonotic diseases. Increased funding in veterinary research is accelerating innovation, and the integration of digital technologies is enhancing disease monitoring and real-time data sharing. A collaborative approach between veterinary and human healthcare sectors is also advancing One Health initiatives for more effective disease management.
Growth by Regional Market Segment
North America led in 2024 with a 35.7% share, driven by disease prevalence, advanced infrastructure, and strong policy support. The U.S. dominates with robust government programmes and widespread pet insurance adoption.
Europe ranks second,backed by high pet ownership, sustainable regulations, and EMA-led access initiatives. The UK leads with high
gment
pet insurance coverage; Germany sees steady growth with strong R&D and livestock base.
Asia Pacific is growing fast with rising R&D, affordable vet care, and government-backed disease control. India is expanding with increased funding, digitisation, and regulatory support for vaccine security.
Latin America benefits from healthcare reforms, rising awareness, and government support. Brazil drives growth with large pet ownership and a strong livestock industry.
The Middle East and Africa are growing due to disease outbreaks and food security needs. South Africa is focusing on poultry health and rabies control through targeted programmes.
Indian Animal Health Industry
The Indian animal health market is estimated at USD 1.97 billion in 2024 and is projected to grow at a CAGR of 13.9% from 2025 to 2030. Growth is driven by rising government support, increasing product launches, evolving regulations, a thriving startup ecosystem, growing R&D investments, and tech adoption.
Recent developments reflect this momentum. In + 2025, the Union Cabinet approved a revised Livestock Health and Disease Control Programme (LHDCP) with a budget of INR 3,880 crore (USD 453 Million). Key focus
areas include mass vaccinations, mobile veterinary units, and the distribution of affordable medicines under the Pashu Aushadhi initiative.
India is also strengthening disease preparedness. In November 2024, the government launched a USD 25 Million animal health security project with G20 funding and support from the ADB, World Bank, and FAO. It aims to upgrade labs, modernise surveillance, and digitise data systems by 2026.
Progress on the regulatory front includes the removal of the outdated TABST vaccine test by the Indian Pharmacopoeia Commission in July 2024, aligning India with global best practices in animal welfare.
The country is also embracing digital solutions. In May 2024, the Department of Animal Husbandry signed an MoU with UNDP to use AI for vaccine tracking and to deploy UNDPs Animal Vaccine Intelligence Network (AVIN) to enhance livestock immunisation and insurance coverage.
Megatrends
Shifting Consumer == Behaviour Driving Pet Care Premiumisation
India is witnessing a surge in pet ownership, particularly among nuclear families and urban youth. This shift is fuelling demand for premium pet nutrition, preventive healthcare, and responsible ownership practices such as spaying and neutering.
Pet parents are increasingly prioritising regular check-ups, tailored diets, and wellness solutions, reshaping the animal health value chain.
==
Digital Acceleration ^== Transforming Animal Health Access and EngagementDigital adoption is rapidly transforming the sector, with tech-enabled startups leveraging IoT, e-commerce, and direct-to-consumer models. These platforms are improving awareness, access to care, and personalised pet solutions, driving the rise of digital-first animal health brands and services across urban India.
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Government Focus Strengthening Veterinary Infrastructure and InnovationFavourable government initiatives, such as increased funding, vaccination programs, and the launch of digital approval platforms like Nandi, are reinforcing the regulatory ecosystem and encouraging innovation. These efforts are critical to improving livestock health, boosting veterinary drug development, and supporting the sectors long-term growth.
Hikal - Business Review of the Animal Health Division
Our Animal Health business continues to grow steadily, not merely as a manufacturer but as an integrated development partner to global innovators, supporting early-stage process development, validation, and lifecycle management of differentiated APIs. With strategic sourcing and backward integration for key intermediates, we help global animal health companies de-risk their supply chains while maintaining cost and quality controls. For animal health innovators navigating increased scrutiny on API traceability, we offer transparent supply chains, cGMP-compliant quality systems, and robust documentation, helping ensure market access and regulatory continuity.
With rising demand for pet care and livestock productivity, we are augmenting capacity and diversifying product platforms to support global growth in veterinary medicine.
We continue to enhance our digital manufacturing practices to improve yield, impurity control, and operational throughput, critical levers in API manufacturing. Our animal health operations also emphasise green chemistry, solvent recovery, and effluent management, aligned with the principle of protecting animal and environmental health together.
Under a long-term agreement with a leading innovator customer, we have successfully completed validation for eight products and are on track to complete a few more. These efforts support product registration and will enable commercial launches in global markets in the coming quarters. Our proven execution of technology transfer and rapid scale-up across multiple products has helped partners derisk commercialisation and meet regulatory timelines globally.
This partnership has acted as a force multiplierearly wins brought new inquiries and opportunities from other innovator customers. As a result, we are now engaging with multiple global clients and building a healthy pipeline of high-value projects.
We are also expanding our capabilities into process development and synthesis of complex molecules. Early results have been encouraging and reinforce our reputation as a reliable partner in differentiated chemistries. With rising demand for veterinary therapeutics, tighter regulations, and a global shift toward innovation-led outsourcing, the Animal Health segment presents strong longterm growth potential.
Global Crop Protection Industry
According to IMARC, the global crop protection chemicals market was valued at USD 96.05 billion in 2024 and is expected to reach USD 141.69 billion by 2033, growing at a CAGR of 3.96% (2025-2033). North America leads with over 39.9% market share in 2024. Key growth drivers include the rising global population, projected to reach 9.7 billion by 2050, and the need for higher crop yields from limited arable land. Soil degradation, climate-
induced pest pressure, and changing dietary preferences are pushing demand for effective pest and disease control.
Technological advances like precision farming, improved formulations, and integrated pest management are supporting market expansion. Government support, increasing farmer awareness, and the shift toward sustainable, bio-based solutions are shaping the future of the industry.
In the U.S., adoption of advanced farming technologies, GM crops, and a focus on maximising yield are major factors. Climate variability and increased pest outbreaks have raised the demand for reliable chemical solutions, backed by research investments and evolving regulatory support.
Growth by Product Type
Herbicides make up about 42% of the global crop protection market in 2024. Their strong position is due to the need for effective weed control, as weeds can reduce crop yields by nearly 28%. The growth of farmland and modern farming practices has further driven herbicide use. Farmers also rely on herbicides to fight resistant weeds, which are becoming a bigger issue worldwide. Herbicides work well across different types of crops and weeds, making them a top choice.
The herbicide segment is expected to grow at a CAGR of about 5% from 2024 to 2029. This is supported by increasing weed-related crop losses and the need to improve yields. The rise of conservation agriculture, better herbicide formulations
for resistant weeds, and new application technologies are boosting demand. Greater farmer awareness and rising food needs globally are also fuelling this growth.
Insecticides protect crops from insect pests, especially in areas affected by climate change.
Fungicides help manage fungal diseases, mainly in humid climates. Molluscicides I control snails and slugs, and nematicides target soil pests that harm roots. Together, these tools support integrated pest management for better crop health and productivity.
Growth by Region
North America dominates the global crop protection chemicals market with over 41% share in 2024. Growth is led by large- scale farming and a shift to biopesticides as stricter EPA regulations take hold. The U.S. market alone is expected to grow at ~6% CAGR, reaching USD 40.1 billion by 2034.
In Europe, the move toward organic farming is accelerating, driven by the EUs Green Deal goal of cutting chemical pesticide use by 50% by 2030.
Asia Pacific is the fastest-growing region, with a projected CAGR of 3.07%. Growth is fuelled by large-scale farming in India and China, rising food security efforts, and continued reliance on synthetic pesticides.
Latin America, led by Brazil, is adopting precision agriculture tools like drones and satellite tech to optimise pesticide use and reduce environmental impact.
The Middle East and Africa are expanding steadily, with countries like South Africa using specialised chemicals to protect crops from extreme weather and ensure stable food production.
Indian Crop Protection Industry
Indias crop protection chemicals market is expected to grow from USD 2.59 billion in 2025 to USD 3.21 billion by 2030, at a CAGR of 4.35%.
As farming practices evolve, Indias agriculture is increasingly adopting modern and sustainable techniques. About 20.8% of cultivated land is used for oilseeds, showing strong potential for crop protection solutions. Farmers are now using precision farming and integrated pest management, especially for commercial crops.
Key market trends include the rising adoption of precision farming and integrated pest management, growing demand for bio-based and sustainable solutions, increased use of insecticides driven by persistent pest pressures, and a shift towards targeted, technology- enabled strategies to improve farm productivity.
The market is facing growing pest-related losses. In 2022, pesticides accounted for 72.5% of the market, as farmers tackled pests like aphids, stem borers, and armyworms. Rice alone faces annual losses of USD 296.1 Million due to root- knot nematodes. Across all crops, 21.3% of yield losses are caused by plant parasitic nematodes, leading to economic losses of USD 1.58 billion.
Despite these challenges, targeted solutions are showing success. In Kodagu, Karnataka, strategic molluscicide use across 300 acres helped reduce mollusk infestations by 90%, improving outcomes for 40-45 plantations. Rising farmer awareness and the development of pest-specific products are helping improve productivity nationwide.
Hikal - Research and Technology Review
Elevating Capabilities
We continued to enhance our commercial and technical capabilities to meet evolving customer needs and ensure scalability from lab to pilot to plant. As a technology-driven partner in pharmaceuticals and crop protection, Hikal invests 4-5% of annual sales in Research & Technology (R&T), with a strong emphasis on safe, efficient, and eco-friendly processes.
During the year, we commissioned a Reaction Calorimeter facility (May 2024) at our R&T Centre, equipped with Mettler Toledo RClmx.
This advanced tool enables safe scale-up by accurately determining thermal profiles, including MTSR, heat of reaction, and accumulation. By bringing this capability in-house, we are reducing outsourcing costs and development timelines, while strengthening our ability to assess thermal hazards early in the process development stage.
We also expanded lab infrastructure and invested in advanced analytical tools to support high-complexity chemistry, aligning with our long-term focus on innovation and quality.
Process Improvement
During process development, we focus on reducing cycle times and solvent usage by recycling recovered solvents, with the goal of minimising waste and its longterm environmental impact.
Filings
Our R&T team filed two US Drug Master Files (DMFs) and completed one Certificate of Suitability (CEP) to the European Pharmacopoeia, along with six CEP amendments and six US DMF amendments for the pharmaceutical segment.
Advancing Innovation in Animal Health APIs
As part of our portfolio expansion, we are making significant progress in developing Animal Health APIs. Several APIs developed by our R&T team have been successfully validated at our new Animal Health Manufacturing facility in Panoli, with validation for additional APIs currently underway. We have filed patent applications for three of these APIs, covering the innovative processes developed by R&T, and submitted related journal articles for publication.
Additionally, we have initiated the development of two Complex Chemistry Molecules in the Animal Health segment. For the one molecule, process development is ongoing at R&T, with validation planned at our manufacturing facility. The second molecule is being validated at the Kilo Lab, with initial customer supply in progress, followed by further process optimisation and commercial scale validation.
Embedding Green Chemistry in Animal Health API Development
We apply Green Chemistry principles in the development of our Animal Health APIs, reinforcing our commitment to sustainability. Several APIs were successfully developed alongside ongoing projects, with plant-scale validation completed at Unit 2. The completion of multiple API developments demonstrates our technical strength and consistent focus on environmentally responsible solutions that deliver both efficacy and positive environmental impact.
CDMO
During 2024-25, the CDMO team has secured a repeat order for a hazardous Click Chemistry project and are preparing for larger-scale batches at Unit 2.
We also completed batches in a cryo reactor for a customer project, safely handling highly pyrophoric butyllithium solution.
Innovation, Safety and Sustainability in Process Development Scaling Click Chemistry with Safety
We reached a major milestone by successfully developing and scaling Click Chemistry for large- scale application, becoming the first in India to do so with stringent safety protocols in place. This reflects our strong focus on both innovation and safe operations.
Process Development for a Flavouring Agent
Our team developed a robust synthesis route for a flavouring agent, laying the groundwork for future scale-up. This achievement reinforces our focus on delivering high-quality, customer-aligned solutions.
Greener Processes for Advanced Intermediates
We created an environmentally sustainable process for an advanced intermediate by eliminating hazardous reagents and enhancing both Process Mass Intensity (PMI) and throughput, demonstrating our commitment to greener and more efficient manufacturing.
Establishing a Process Safety Lab
A new Process Safety Lab was set up at our R&T centre, equipped with advanced tools such as Reaction Calorimetry, Gas Evolution Kit, HF-Cal, and DSC. A dedicated team of scientists oversees the lab to drive safe innovation and process reliability.
Zero Liquid Discharge (ZLD)
We undertook a project to achieve zero liquid discharge (ZLD) at our facility. We have successfully installed and commissioned a 30 KLD Ultrafiltration (UF) and Reverse Osmosis (RO) plant, along with a 10 KLD Mechanical Vapour Recompression (MVR) system followed by an Agitated Thin Film Dryer (ATFD).
Crop Protection
Our dedication to innovation and process optimisation has led to remarkable achievements this year.
As part of our R&T strategy, we will continue to prioritise customer-recommended and in-house product developments, with a focus on effective commercialisation. Our aim is to convert contract development projects into long-term manufacturing opportunities across the pharmaceutical and crop protection divisions.
To enhance product competitiveness, we areimplementing process improvements, productivity measures, and cost-reduction strategies. We continue to invest in advanced technologies and forge strategic partnerships to support these efforts.
Our commitment to newer, greener technologies will help reduce our carbon footprint, optimise resource use, and improve overall process efficiency.
Financial Review
Consolidated Abridged Profit and Loss Statement
| Particulars | 2024-25 | 2023-24 |
| Total Revenue | 18,598 | 17,846 |
| EBITDA | 3,335 | 2,694 |
| PBT | 1,239 | 954 |
| PAT | 909 | 695 |
Cash Flow Position
As of 31 March 2025, cash flow position is strained on account of market dynamics predominantly driven by increased account receivables by four days. The Company generated INR 2,804 Million from operating activities, a increase from the previousyears figure of INR 1,866 Million. The Companys investing activities resulted in a cash outflow of INR 1,365 Million, which was utilised to expand capacity as part of Hikals ongoing capex programme aimed at realising future business opportunities.
Meanwhile, financing activities led to a outflow of INR 1,436 Million, indicating an degrade Cash Flow from the previous years figures. As of 2024-25, the Companys closing balance of cash and cash equivalents stood at INR 129 Million.
Commentary o
Improved cash flow on account of significantly high operating profit coupled with controlled capital expenses towards assets.
Debt Position
In 2024-25, the net-debt equity ratio has decreased to 0.59 compared to 0.67 in the previous year. The interest cost incurred during the current fiscal year was INR 752 Million, indicating an increase from the previous years interest cost of INR 564 Million.
Commentary
Long-term debt repayment and capital expenditure was funded largely through the internal accruals resulted in improved debt equity ratio. v
Return on Equity (RoE) and Return on Capital Employed (RoCE)
2024-2025 saw an increase in the Return on Equity (RoE) to reach 7.41% compared to the previous years figure of 5.99%. The Return on Capital Employed (RoCE) has also increased by 204 bps from 7.69% in 2023-24 to 9.73% in 2024-25.
Commentary ?
Improved profitability on account of cost improvement initiatives and operating leverage has culminated in improved returns.
Capex
For 2024-25, we have allocated a total of INR 1,373 Million towards a Capex programme aimed at increasing capitalisation. The funds will be used to create multi-product plants that will benefit both the Pharmaceutical and Crop Protection divisions, as well as upgrade the infrastructure of existing production facilities.
Commentary
We anticipate that these new plants will reach full capacity utilisation within next 2-3 years. We are committed to the Capex investment for capitalising on long term growth opportunities such as emerging Animal Health business.
| Consolidated Cash Flow Statement | (INR in Million) | |
| Particulars | As on 31 March 2025 | As on 31 March 2024 |
| Opening Cash and Cash Equivalents | 126 | 267 |
| Cash flows from | ||
| (a) Operating Activities | 2,804 | 1,866 |
| (b) Investing Activities | (1,365) | (1,737) |
| (c) Financing Activities | (1,436) | (270) |
| Closing Cash and Cash Equivalents | 129 | 126 |
Key Financial Ratios
| Particulars | As on 31 March 2025 | As on 31 March 2024 | Variance (%/bps) |
| Debtor Turnover | 3.46 | 3.59 | 4 |
| Inventory Turnover | 2.62 | 2.66 | 1 |
| Interest Coverage Ratio | 4.44 | 4.78 | 7 |
| Current Ratio | 1.26 | 1.28 | 1 |
| Net Debt Equity Ratio | 0.59 | 0.67 | 12 |
| Net Profit Margin (%) | 4.90 | 3.90 | 26 |
| Net worth | 12,622 | 11,876 | 6 |
Strategic Review
Project Pinnacle
Project Pinnacle is our business transformation initiative designed to advance the next phase of our growth strategy and strengthen our operational pipeline. Now in its third phase, the project is continuing its results, driving sustainable growth through supply chain momentum, de-risking measures, differentiated capabilities, global customer acquisition, and the development of a robust technology platform.
I Leadership in ESG
In line with our purpose of improving lives and serving the community, we are committed to embedding sustainability across all aspects of our operations.
As part of our ESG framework, we continuously identify areas for improvement and engage with global rating agencies to benchmark our progress.
Our efforts have earned us notable recognition, including a Bronze Medal from EcoVadis at an organisation level and inclusion in the CDP B List. Looking ahead, it will continue to be a strategic priority, supported by a defined roadmap to drive lasting environmental and social impact.
In 2024-25, we submitted the UNGC Communication on Progress (CoP) report and carried out BRSR limited assurance. We also initiated GHG Scope 1, 2, and 3 emission accounting for the current year as part of our commitment to submit nearterm SBTi targets by the end
of 2025-26. Implementation of the SBTi roadmap is already underway.
We made significant strides in energy sustainability, with 77% of our electricity consumption met through renewable sources. A comprehensive safety diagnostic study was conducted by a renowned consultant to enhance our inherent safety strategy at manufacturing facilities.
We are also embedding ESG considerations into our technology selection process for upcoming projects, such f as, we adopted automatic
vertical plate filters, electrically operated diaphragms, and water- based PU paints, technologies chosen for their lower environmental footprint.
Initiatives Undertaken
Key Account Management (KAM) Systems
We enhanced our KAM approach across multipleaccounts to build deeper strategic relationships.
As part of our KAMs, we have:
Defined priority accounts basis current size and full potential
Defined key roles and responsibilities to manage priority accounts and ensure delivery excellence
Developed a mechanism to consistently ensure customer delight
Customer Roadshow
Roadshow through strategic locations across the globe, including Japan, South Korea, Europe, the US, and Latin America
It is an opportunity to engage with senior leadership from our existing esteemed clientele while forging new connections with potential customers
It will help in paving the way for future partnerships that will be instrumental in realising our vision
Regulatory Compliance
We are committed to green chemistry and engineering and continue to invest in processes and systems that enable safe, responsible operations in line with global regulatory standards.
Competitive Advantage
Our production plants are compliant with international agencies like the US FDA, PMDA, EU, and other global agencies.
We Use it
To create shared value and maintain business sustainability
To align our interests with collective well-being
Risk Management
At Hikal, we believe that managing risks is a vital part of our overall strategy. It enables us to operate efficiently and meet our goals. We recognise that effective risk management is essential to achieving our objectives. That is why we proactively identify and mitigate potential risks.
This approach allows us to embed risk management into our Company culture. We consider it not just a requirement but vital for successfully navigating our business challenges.
Since implementing a structured risk management approach in October 2021,
we have observed significant improvements in areas such as Supply Chain Management, Business Continuity Planning, Compliance, Financial Oversight, and Information Technology. This approach equips us to tackle challenges and accomplish our strategic goals.
Risk Management Objectives
To ensure that all our current and future material risk exposures are identified, assessed, quantified, appropriately mitigated, and managed, i.e., to ensure adequate and robust systems for risk management.
To ensure compliance with appropriate regulations, including those related to ESG, through the adoption of best practices.
To ensure business continuity and sustainable growth with financial stability.
Risk Management Process
An effective risk management process requires continuous and consistent assessment, mitigation, monitoring, and reporting of risk issues across the full breadth of the Company. All senior executives, under the guidance of the Managing Director, are responsible for monitoring managements processes and results in identifying, assessing, and managing risks. The risk management process adopted by us has been tailored to our business processes, with reference to ISO 31000 and the COSO ERM frameworks.
Hikal Limiteds focus is on mitigating risks towards meeting the following broad objectives:
Broadly categorising, the risk management process consists of the following stages/steps:
Risk Assessment (Identification, Analysis and Evaluation)
This involves identifying risks and likely causes that could affect the Companys objectives. Risk evaluation involves comparing the level of risk identified during the analysis process with the predefined risk weight to assess the potential severity of impact and the probability of occurrence.
Risk Profile
We regularly monitor the identified risks using Key Risk Indicators (KRIs) and Key Performance Indicators (KPIs). In our Group meetings with Risk Champions, we analyse and discuss each risk to encourage ongoing conversations about managing them. We reassess the risks based on feedback from the Management Committee. This continuous evaluation has resulted in Hikals risk register listing 19 different risks, with six rated as catastrophic, six as significant, two as moderate, three as low, and two as negligible.
Risk and Response
| Risk Description | Action Taken |
| Non-complying with PCB consent and hazardous waste guidelines | Implemented an online monitoring system for effluent and boiler stack across all Hikal sites A digital information Board providing updates on environmental and safety issues was installed at each facilitys entrance Quarterly EHS compliance audits were conducted of all sites |
| Unsafe practices and deployment of workforce (Company and Contractor) in non-specified areas leading to accidents | Safety programmes, including plant safety inspections, safety meetings, one-minute safety tips, and near-miss reporting, have been organised to ensure participation from all employee levels Globally Renowned Consultant has been appointed to lead the safety culture transformation initiative |
| Issues arising from USFDA inspection may adversely impact Company revenue, reputation, etc. | We are currently reviewing our policies and procedures to ensure that all activities are in full compliance with USFDA requirements, and we expect to receive clearance from them soon |
| Delays in regulatory approvals and meeting compliance requirements pose challenges to the rapid growth of the business | An effective governance system is established, ensuring that compliance status is regularly updated to the relevant authorities and corrective actions are taken promptly |
| Challenge in achieving revenue growth from non-Gaba products | The pharma business expanded geographically into new countries. We have initiated transactions with numerous new customers over the past two years |
| Difficulty in achieving revenue growth from existing products and meeting budgeted targets for new products | We have strengthened several processes, including KAM, customer feedback, customer risk assessment, and salesforce utilisation, to address this risk |
| Crisis and Risk Management | A crisis communication plan was implemented, and training was given to all concerned, including business unit heads |
| Risk of business loss due to natural disasters | On-site emergency plans were evaluated for all locations. Identified gaps were addressed. The effectiveness of on-site emergencies is ensured through periodic mock drills. In addition, capital expenditures were allocated to each site to enhance preparedness for handling potential flood situations |
| Lack of Disaster Recovery Plan (DRP) leading to revenue and productivity loss | An IT DRP drill is conducted at regular intervals The process is set up to store PLC programme backup in the cloud The DR system for the ERP application has been developed |
| Business uncertainty or loss of receivables due to transacting business in countries where political and economic conditions threaten trade | The credit insurance policy was renewed with an adequate amount of coverage The Company implemented Hikals revised credit policy The Company engages in secured transactions with high-risk countries |
| Monopoly/ limited suppliers for raw materials | Alternate vendors were developed to mitigate risk and reduce prices We have nearly eliminated our reliance on monopolistic suppliers in the Crop division |
| Any geographic risk in China may significantly affect Hikals operation | We are working to develop alternative vendors outside China whenever possible. Additionally, we are closely monitoring geopolitical shifts and ensuring our operations continue uninterrupted |
| Risk Description | Action Taken |
| Develop new (modified) products or services within the anticipated timeline and budget (R&T) | The timesheet application has been developed, and the deployed resources timing is logged in the timesheet The Company is streamlining the process of estimating project costs |
| Project Costs and Schedule Overruns | The Company emphasises its Be one team philosophy, and all relevant departments work in good coordination while following standard processes. Periodic project workshops are conducted to prepare mitigation strategies for identified project risks. The Company ensures that budget revisions comply with the requirements of the DOA |
| Exposure to a cyber-attack in the absence of updated security measures | We have IT protection systems, including SOC, Firewalls, Barracuda, CrowdStrike, Patches, and Zscaler. The responsible individuals are tasked with monitoring and addressing alerts as a priority for these protection systems |
| Attrition level is high in junior and middle management cadre due to high demand | The Company is centred around three main areas: culture, capability, and connection, also known as the 3Cs. The HR department is implementing specific initiatives in each area to ensure maximum impact. The Company has redefined its attrition matrix to control attrition better, resulting in an increased risk rating |
| Unutilised GST input credit in Maharashtra | Unused GST input credit is steadily decreasing due to credit allocation to other states and the strict monitoring of sales and purchase transactions |
| Increase in interest rate will impact profits | The interest rate has steadily increased over the past four years. However, it remains more favourable than the market rate. The Company has taken various measures to mitigate interest rate risks, including establishing relationships with new lenders to obtain competitive rates, ensuring sufficient line availability across all lenders, negotiating more favourable terms and pricing, and exploring alternative financing sources |
| The adverse impact due to Foreign Exchange Volatility | The Treasury Department monitors Forexs position daily and reports to the Board every quarter |
Human Resources
Our people are integral to our long-term growth and operational excellence. In 2024-25, we continued to strengthen our human capital through focused efforts in inclusion, employee well-being, learning and development, and workplace safety.
We maintained a strong emphasis on diversity and equal opportunity, with structured initiatives such as the Womens Forum, MD Connect sessions, and leadership engagement platforms. Our wellness programme Ojas and employee engagement platform Uday supported physical and mental well-being across locations. High-performing individuals and teams were recognised through the Parigyaan awards framework.
Skill development remained a key priority, with over 44,521 training hours delivered through technical, behavioural, and digital learning formats, including LinkedIn Learning. Programmes focused on safety, compliance, leadership, and functional capabilities were implemented
across levels. Safety performance was further strengthened through structured interventions, including the 21-Day Safety Challenge, site-specific mock drills, and expanded digital reporting systems.
We upheld our commitment to human rights through robust governance mechanisms, awareness sessions, and policy enforcement. Grievance redressal, anti-discrimination measures, and adherence to global labour standards remain core to our people practices.
Internal Controls and their Adequacy
The Company is dedicated to maintaining an independent and objective internal audit function that operates across all sites and business units. The mission of Hikals Internal Audit Department is not just a function but a crucial pillar of the Companys success.
It plays a vital role in assisting management and the Board in achieving their objectives by employing a systematic and disciplined approach to evaluate and enhance the effectiveness of Hikals governance, risk management, and internal control processes.
Objectives of Hikals Internal Audit Department
Assist the organisation in fulfilling its governance responsibilities
Ensure the adequacy of controls within Hikals systems and activities and bring any deficiencies to the attention of operational management and, ultimately, the Audit Committee or relevant authorities.
Advise management on cost-effective controls for new or modified systems and activities.
Identify opportunities to reduce costs through improved efficiency within systems and activities.
Examine whether employees actions comply with policies, standards, procedures, and applicable laws and regulations.
Support management in developing risk management strategies for business risks.
Assist management in standardising departmental processes.
Stay updated with industry best practices and emerging trends.
The Internal Audit Department assesses the adequacy and effectiveness of internal control systems using a systematic and disciplined approach. It collaborates with management to challenge and enhance existing and proposed practices while suggesting ideas for process improvements.
The Management Committee ensures the establishment of internal controls that effectively comply with relevant laws and regulations. Procedures are in
place for the timely detection of errors and fraud. Management is accountable for taking prompt and appropriate actions to address any control issues or risks that exceed acceptable limits.
The Internal Audit Department has completed all audits as per the audit plan for the fiscal year 2024-25. Audit reports were discussed with the management committee and audit committee on a quarterly basis, and appropriate actions were taken to address all audit findings.
Additionally, the Company has implemented an internal control system that includes entity-level controls, Information Technology General Controls, and financial and operating controls. Operational effectiveness testing of these controls over financial reporting was performed for the fiscal year 2024-25, as mandated by SEBI Regulations and the Companies Act, 2013, with satisfactory performance noted for all these controls.
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