More than medicines.
We manufacture trust.
A global CDMO partner, grown from the hills of Himachal Pradesh — developing and manufacturing pharmaceuticals, nutraceuticals, cosmeceuticals and herbaceuticals for the companies the world trusts with its health.
20+ years of disciplined manufacturing habit.
Founded in the hills
Incorporated with a single manufacturing unit in Nalagarh, Himachal Pradesh — the foundation for everything that follows.
First global standard
WHO-GMP certification achieved within a year — the first of 30+ accreditations to come.
An international partner
Malaysia's Hovid takes a 51% stake, opening Southeast Asian markets and shared know-how.
Independent, ambitious
Mr. Anurag Kumar completes a 100% acquisition, setting an independent, quality-led path.
VITAGEN is born
The VITAGEN nutraceutical brand launches across general, sports and medical nutrition.
Trusted by the majors
Manufacturing begins for global names, including the Sanofi Allegra franchise.
Thirty, and counting
Crosses 30+ accreditations across pharma, quality, lab, food and trade.
Backed for the next phase
Health Canada approval and a ₹110 Crore Piramal Alternatives investment accelerate growth.
A global CDMO
Two facilities, a DSIR-approved R&D centre, and products reaching 56 countries.
Built by people who've made it from the ground up.
“We don't make medicines to a price. We make them to a standard the next marketwill demand of us.”
Mr. Anurag Kumar took full ownership of Biodeal in 2015 and has driven its growth from a single plant into a globally accredited CDMO — building the quality systems, the DSIR-approved R&D depth, and the partnerships that now carry the company across 56 countries.
His conviction is simple: manufacturing is never a commodity. It is the promise behind every dose — and the reason global majors and first-time founders alike choose Biodeal.
— Mr. Anurag Kumar, Managing Director
Leads end-to-end production across both Himachal Pradesh facilities, from oral solids to sterile lines.
Owns WHO-GMP, PIC/S and Schedule M compliance, and dossier support for export filings.
Runs the DSIR-approved development centre — formulation design through technology transfer.
Drives contract manufacturing, loan licensing and brand partnerships across India.
Manages registrations and supply across 56 export markets in six regions.
Stewards the ₹110 Crore Piramal Alternatives investment and the growth plan.
Names, portraits and bios are placeholders — to be supplied by the client.
Be healthy together.
Three commitments sit beneath everything we make — to the people who take our products, the places we operate in, and the communities we're part of.
Health
Quality that holds up to the world's strictest regulators — because every dose carries someone's trust. WHO-GMP and PIC/S as the floor, not the ceiling.
Environment
Built in an eco-friendly, pollution-free belt — with responsible water, effluent and energy practices engineered into every line.
Society
Skilled science careers in the hills, and access to affordable, dependable medicine across fast-growing emerging markets.
Serving 56 countries across six regions.
From our WHO-GMP and PIC/S certified facilities in Himachal Pradesh, Biodeal exports to distributors, brands and government health agencies across six regions. Hover a country, or select a region to explore.
six regions
Two facilities. End-to-end manufacturing depth.
Two factories and ten manufacturing units across 19.5 acres in Himachal Pradesh give Biodeal unusual range — from high-volume oral solids to one of pharma's most demanding categories, sterile injectables — all under one quality system, with a USFDA-compliant nasal plant on the way.
Orals, nutra, herbal & nasal
Our founding facility runs the broadest spread of dosage forms — manufactured under WHO-GMP and Schedule M compliant conditions.
Sterile & injectables
A dedicated facility for one of the most technically demanding categories in contract manufacturing — aseptic processing in validated clean rooms, and expanding.
USFDA-compliant nasal plant
A dedicated nasal, nutra and herbal facility under build-out — engineered for US-market compliance and the next tier of regulated markets.
DSIR-approved development
Formulation design and stability studies through CTD/ACTD dossier prep and technology transfer — concept to commercial launch, in-house.
Certified to export, everywhere
WHO-GMP and PIC/S credentials streamline filings in destination markets — the same quality regime on every batch.
Tell us what you need to make.
A focused brief gets you a routed answer from the right team within one working day.