End-to-end CDMO — development to commercialisation.
From DSIR-approved formulation R&D to nasal spray and sterile injectable manufacturing, packaging and quality release — Biodeal is the single, accountable partner that carries your product from concept to commercial scale.
Seven capabilities under one quality system.
From contract manufacturing to specialist intranasal and sterile delivery — every service runs on the same WHO-GMP and PIC/S certified backbone, so quality never changes when scope does.
Nasal Spray CDMO
India's leading nasal spray CDMOThe full range of intranasal delivery — metered-dose, aqueous, herbal, nicotine BP, saline, antihistamine and corticosteroid sprays — manufactured with advanced fill-and-seal technology in validated clean rooms.
Contract Manufacturing
Third-party manufacturing across tablets, capsules, oral liquids, dry syrups, injectables, nasal sprays, nutraceuticals and herbals — scalable for domestic and export volumes across both facilities.
Injectable CDMO
Sterile & aseptic manufacturing — SVP vials and ampoules, lyophilised injectables and sterile fill-finish under validated Grade A/B clean room conditions, for domestic and export markets.
Research & Development
Our DSIR-approved R&D centre takes a molecule from formulation design and stability studies through CTD/ACTD dossier preparation to technology transfer — concept to commercial launch.
Loan Licensing
The fastest, most cost-effective route to market for marketing companies and new brands — access our WHO-GMP facility, quality systems and drug licences without investing in manufacturing infrastructure.
Nutraceutical CDMO
Softgels, gummies, effervescent tablets, protein powders, sachets and functional foods — manufactured under WHO-GMP and ranked among India's Top 10 Nutraceutical Contract Manufacturers in 2023.
Herbaceutical CDMO
Tradition meets GMP precision — herbal capsules, AYUSH syrups, standardised botanical extracts, herbal nasal sprays and churna powders, for Ayurveda, naturopathy and wellness brands.
One accountable line from lab bench to loading dock.
Every engagement moves through the same disciplined lifecycle — so a molecule that starts in our R&D centre is the same molecule that leaves our dock, fully documented and quality-released.
R&D
Formulation design, prototypes and stability testing at our DSIR-approved centre.
Regulatory dossier
CTD/ACTD dossier preparation, analytical validation and registration support.
Pilot batch
Small-scale pilot runs for regulatory submission and market testing.
Commercial mfg
Full commercial production on dedicated, category-separated lines.
Filling & packaging
Automated filling and sealing, multiple formats, serialised labelling.
Quality release
In-process and finished QC, with a Certificate of Analysis for every batch.
Can we make your volume? Almost certainly.
Two facilities, 28 production lines and billions of units a year. Here is the throughput buyers ask about first — line counts and annual capacity, before anything else.
High-volume oral solids and liquids alongside nasal, nutraceutical and herbal lines — all under WHO-GMP and Schedule M.
A 14-acre sterile campus built around a Grade A/B aseptic core, with its own water-for-injection and pure-steam utilities.
Launch your brand — without a factory.
Access our WHO-GMP certified facility, quality systems and drug licences under your own brand name, with no capital tied up in manufacturing infrastructure. Four steps from product list to dispatch.
Start loan licensing
Share your brief
Submit your product list, brand details and target markets to Biodeal.
Feasibility review
Our R&D and regulatory team assesses formulation feasibility and requirements.
Manufacture
Products are made at our licensed facility under your brand name.
Dispatch
Finished goods ship direct to your warehouse, distributor or C&F agent.
Request a manufacturing proposal.
Tell us your product category, dosage form, target markets and volumes — our team responds with capacity availability and a preliminary manufacturing proposal within 48 hours.