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Syngene is well positioned for accelerating growth and transformation, with the potential to become a leader in serving the global biopharma and wider life sciences outsourcing market models.

Dear Shareholders,

Let me first say how honored I am to be back at Syngene after almost ten years, and it is especially exciting to return at such a dynamic time in the CRDMO industry and to have the opportunity to contribute to Syngene’s on-going growth story.

Syngene’s integrated and comprehensive end-to-end capabilities differentiate us in our ability to strategically support customers in the pursuit of their R&D and manufacturing goals. While Syngene’s roots lie in early-stage research and development, we have continuously strengthened our offerings through investments in new technology, capabilities, capacity and of course the talent and experience of our skilled scientists and workforce. Building manufacturing platforms for both small and large molecules has enabled us to straddle the entire value chain, and we have taken recent strategic steps with the acquisition of new facilities to further augment capacity as well as increase efficiencies and productivity.

This year’s theme for our annual report, ‘Innovating Reach – Researching New Paths, Delivering Breakthroughs’, reflects well our continuing evolution in expanding Syngene’s service offerings into exciting new modalities at the leading edge of contemporary medical research and development including protein production platforms and expansion of our research capabilities into areas such as antibody-drug conjugates, peptides and oligonucleotides.

Performance this year

As we had guided, FY25 was a challenging year of two distinct halves. In the first half, performance was muted driven by a sectoral downturn in U.S. biotech funding that affected our Discovery Services division, while in the second half we saw a recovery in Discovery Services as funding returned, building on top of growth momentum in both our small and large molecule manufacturing divisions. Overall, we delivered a resilient performance in a challenging year.

A key dynamic for the year was the marked increase in customer RFP’s as they explored alternative options to rebalance their CRDMO business exposure away from China. Typically, these customers set up ‘pilot studies’ across a range of services, often placing them with a select short list of companies. The pilot studies are then used as the basis for customers to select longer term partners to undertake more substantial program work. I am very pleased to report that Syngene has been achieving a high success rate of conversion and that the pipeline of pilot studies has a good momentum going into FY26.

Within the CRDMO market, the large molecule CDMO segment has been the fastest growing, driven by the rapid expansion of, and increasing demand for, biologics and monoclonal antibodies to treat cancer and immunological diseases. Syngene identified this area as an opportunity for growth and in the last few years we have made sustained investments to build a strategic large molecule platform capability. This year, we continued our investment commitment to scale up our biologics manufacturing capacity through the acquisition of a facility in Baltimore, Maryland, which is a key biotech hub in the Northeast of the United States.

Highlights of the year included:

  • The acquisition of Syngene’s first U.S.-based biologics site is expected to support monoclonal antibody manufacturing and is expected to be operational in the second half of FY26. This site will increase the Company’s total single-use bioreactor capacity to 50,000L for large molecule discovery, development, and manufacturing services and also provides a strategic foothold in the U.S. customer market. The Company also completed successful The Central Drugs Standard Control Organization (CDSCO) and local FDA inspections for its Biologics Unit 3 in Bengaluru.
  • Introduction of a protein production platform reducing development timelines by several months for a range of biologics including monoclonal antibodies, biosimilars, antibody drug conjugates, and other recombinant proteins, enabling improved speed of delivery to our customers.
  • Expansion of capacity and capabilities in Discovery Services continued at the Bengaluru and Hyderabad campuses, with a focus on antibody drug conjugates, peptides, and oligonucleotides, in anticipation of long-term demand.
  • China-independent supply chain development continued through strategic sourcing from the Indian ecosystem, and engagement with global suppliers to establish operations in India. Introduced 18 months ago, the offering has gained traction, with approximately one-third of RFPs opting for the China-independent supply model.
  • Achievement of 5S certification marked a milestone as Syngene became the first company in the Indian pharma and life sciences industry to receive this recognition for its biologics quality control laboratory. Awarded through a joint evaluation by the Union of Japanese Scientists and Engineers (JUSE) and the Quality Circle Forum of India (QCFI), the certification reflects improved workplace organization, enhanced safety, increased productivity, and strengthened quality control.
  • Securing of a Silver rating on the EcoVadis sustainability index placed the Company in the top 15% of assessed companies. Scope 1 and 2 targets were approved by the Science Based Targets initiative (SBTi) as aligned with the 1.5°C trajectory, with commitments to reduce emissions by 54.6% by FY33 and ensure 81.6% of key suppliers adopt science-based targets by FY28.
Future outlook

Looking forward, it is clear that we face a period that will be characterized by a higher degree of unpredictability and turbulence driven by shifting global geopolitics and geoeconomics. These dynamics will likely influence and shape the balance of headwinds and tailwainds that Syngene will face as we seek to continue our growth story in the CRDMO market.

Notwithstanding this backdrop, the fundamentals of market opportunity for Syngene remain very robust. Syngene’s share of the global CRDMO market is currently less than one percent, indicating clear headroom for growth and market share expansion. India itself is also now clearly seen as a global ‘growth platform’ as revealed in a Boston Consulting Group (BCG) white paper titled, ‘Unleashing the Tiger: Indian CRDMO Sector 2025’ presented at the BioAsia conference in Hyderabad in February this year. Today, India holds only a 2-3% share, or USD 3.6 Bn, of the USD 145 Bn global CRDMO market. But, as the report indicates, there is potential for the Indian industry to grow to USD 22 Bn - USD 25 Bn by 2035 representing a 15% CAGR. This growth is expected to outpace the global industry, driven by India’s increasing capabilities, enhanced capacities, faster startup times, and cost advantage over the West. Recognizing this opportunity, Syngene along with ten other CRDMOs in the country have come together to launch the Innovative Pharmaceutical Services Organization (IPSO)*, which will provide the industry with a platform to drive advocacy, build an ecosystem of innovation, and address critical challenges such as supply chain resilience and regulatory efficiencies.

U.S. manufacturing facility at Bayview, Baltimore, United States

Syngene is well positioned for accelerating growth and transformation, with the potential to becoming a leader in serving the global biopharma and wider life sciences outsourcing market models. Together, working with our partners, our focus remains on delivering exceptional output value and service to our customers to support them in their innovation journeys to bring new products to the market.

In closing, I would like to thank the 8,500 Syngene employees for their dedication and hard work which has underpinned our performance this year and provides the foundation for our future growth.

Peter Bains
Managing Director & CEO

*The association is currently under the registration process.

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