Manufacturing facilities
Where we make it.
Our plant sits at Plot No. 7, Umiya Industrial Estate, Indrad — about half an hour from Ahmedabad. It was designed and is run by a skilled, experienced team, and built to meet the standards of both Indian and global regulators.
What's on site
Six areas, under one roof.
BLOCK A
Bulk API manufacturing
Where we make our bulk active ingredients — the B12 family, plus our heart and metabolic actives — each on its own dedicated, contained line.
BLOCK B
Sterile & freeze-drying
Our clean sterile core, with freeze-dryers that stopper vials inside the chamber. We develop and validate the cycles ourselves, and keep everything sterile from fill to finish.
BLOCK C
Filling lines
Our lines for dry-powder injections and liquid injections, filling anything from 2 ml ampoules up to 100 ml vials.
QC · GLP
Quality control lab
Our own GLP lab checks identity, strength, sterility and stability, and signs off every batch against BP, USP, EP, IP and JP standards.
R&D
Research & development
Our scientists keep improving how we make things — refining routes and freeze-drying cycles to be safer, greener and better value.
STORES
Storage & dispatch
Temperature-controlled stores for raw materials and finished goods, and dispatch that's ready for cold-chain shipments at home and abroad.
We're happy to show you around or host an audit visit — just get in touch to arrange a time.
What we do best
Lyophilisation is our strong suit.
It's written into our mission statement, and for good reason. Freeze-drying is the hardest way to keep a sterile drug stable — and it's why a Decro vial still mixes cleanly at a hospital years after it leaves Indrad. Here's how it works.
- 01
Freeze
−45.0 °C
Shelf temperature
The solution is cooled well below freezing on tightly controlled shelves, so the drug sets into a stable, solid form.
- 02
Vacuum
0.081 mBar
Chamber pressure
Pressure drops to a fraction of a millibar. Under a vacuum this deep, the ice can't melt — it can only turn straight to vapour.
- 03
Sublimate
−20.0 °C
Primary drying
Over primary and secondary drying, the water leaves bit by bit, leaving behind a dry cake that dissolves the moment it's needed.
- 04
Seal
+25.0 °C
Stoppered under N₂
Vials are stoppered under nitrogen and sealed right there in the chamber, so they stay sterile from fill to finish.
The result · sterile lyophilised vials
A stable, dry cake that mixes back cleanly the moment it's reconstituted.
Standards & compliance
Held to Indian and global standards.
Our facility is designed, documented and audited against every framework below — the State FDA and CDSCO at home, and WHO-GMP, EU-GMP and PIC/S for the markets we export to. Every batch is released through our own GLP quality-control lab.
- 01
WHO cGMP
World Health Organization current Good Manufacturing Practices
- 02
EU GMP
European Union Good Manufacturing Practice guidelines
- 03
PIC/S
Pharmaceutical Inspection Co-operation Scheme guidelines
- 04
Schedule M
Indian GMP requirements under the Drugs & Cosmetics Rules
- 05
GLP
Good Laboratory Practices across quality control
- 06
CDSCO
Central Drugs Standard Control Organisation, India
Need certificate scopes or an audit pack? We send them with every quotation — just email sales@decropharma.com.
Get in touch
Looking for a manufacturing partner?
Whether you need bulk APIs, finished injectables or contract manufacturing, tell us what you're after — in India or abroad — and we'll come back with specs, pricing and lead times.