Biotech: Biosimilars, Vaccines and Novel Science
India's biotech strength in biosimilars and vaccines is broadening toward novel therapeutics and bio-services.
Market Size
~$10 Bn (India biotech, FY26E)
Growth
~14% CAGR (FY26–30E)
Read
7 min
Published
Apr 2026
Overview
India's biotechnology sector has historically excelled in vaccines and biosimilars, supplying large global volumes at competitive cost. The industry is gradually broadening toward novel biologics, cell and gene therapy research, and bio-services (contract biologics development and manufacturing). Strong scientific talent and cost-efficient capacity underpin the opportunity.
Biosimilars - lower-cost versions of biologic drugs going off-patent - represent a large, expanding global market where Indian firms are well positioned. Vaccine manufacturing capability, demonstrated at scale, remains a strategic asset. Government support for bio-manufacturing and a growing venture ecosystem are seeding earlier-stage innovation.
Biotech carries higher scientific, clinical and regulatory risk than generic pharma, with longer development timelines and binary trial outcomes for novel work. The biosimilar and bio-services segments offer more predictable, nearer-term returns than frontier therapeutics.
Illustrative projection from the report's stated market size (~$10 Bn (India biotech, FY26E)) and growth (~14% CAGR (FY26–30E)).
Key Highlights
- Established biosimilar and vaccine leadership
- Broadening toward novel biologics and bio-services
- Cost-efficient biologics manufacturing capacity
- Higher scientific and clinical risk than generics
Growth Drivers
- Large global biosimilar opportunity as biologics lose patent
- Demonstrated vaccine-manufacturing capability
- Government bio-manufacturing support and venture funding
- Growth in contract biologics development and manufacturing
Key Players
Investment Outlook
Biotech offers structural growth via biosimilars and bio-services, with novel therapeutics as higher-risk optionality. We favour firms with commercialised biosimilar portfolios and bio-services revenue over pure discovery-stage risk.
Key Risks
- Clinical-trial failure and binary development risk
- Complex regulatory approval pathways
- Long gestation and heavy R&D capital needs
The Neoma View
We prefer biotech exposure anchored in commercialised biosimilars and bio-services, treating novel-therapeutic pipelines as a small, high-optionality overlay.
Talk to an advisor →All figures are indicative and for information only - not investment advice or a recommendation. Market sizes, growth rates and financial metrics are hedged estimates that vary by source and period. Please consult your advisor before investing.
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