We have recently become a part of a CDMO comprising a team of highly experienced and qulified Professionals with vast experience in the field of Manufacturing API’s & Intermediates .
Team comprises members from Top management of reputed Pharmaceutical companies, Chemical engineer,senior organic scientist and regulatory expert.
We have acquired control of Drugs intermediate and API manufacturing Plant situated in Western India with WHO GMP certification.
- Reaction volume capacity 40 KL comparising of Glass lined reaction and SS Ractors.
- 2 nos multipurpose reaction lines and clean room areas
- Capable to undertake reactions likes – Hydrogenetion, Bromination ,Alkylation, Reduction, Condensation and Hydrolysis.
- Flexible Pollution control consents to operate for Intermediates and API,
Discharge to CETP.
Another API manufacturing facility located nearby;
- 3 multipurpose reaction lines.
- Who GMP approved. USFDA and EU GMP complaint
60 KL Reaction capacities capable to handle diverse reactions
- Consent to operate flexible for addition of new products
- Full fledged ETP plant with discharge permission to CETP
Further we have available under our control and management additional 3 manufacturing plants with multiple reaction capabilities.
Plants are WHO GMP approved having discharge permission to CEPT available.
Plants available for inspection / audit with related permission in place.