Six gatesbetween blendingand release.
Any one of them can stop a batch. None can be skipped to protect a delivery date.
- 1
Raw material
Identity and assay of every API and excipient on receipt.
- 2
Blend uniformity
Sampled across the blender, not just from the top.
- 3
Weight and hardness
Checked at fixed intervals throughout compression.
- 4
Disintegration
Release profile verified against the specification.
- 5
Microbiology
Bioburden, and sterility testing for injectables.
- 6
QA release
One named signature carries the batch to market.
What we hold.
Every licence, with its number and validity. The full certificates are in our credential pack, issued for tenders, audits and partner onboarding.
Request the credential packWHO-GMP
Certificate of Pharmaceutical Products — WHO-GMP, State Drugs Licensing Authority
Licence no.GMP/2024/1187Valid to31 Mar 2027
ISO 9001:2015
Quality Management System, Accredited certification body
Licence no.QMS/IN/40912Valid to14 Feb 2028
FSSAI
Central Licence — food & nutraceutical, Food Safety & Standards Authority of India
Licence no.10024022000731Valid to31 Mar 2029
US FDA
Drug Establishment Registration, U.S. Food & Drug Administration
Licence no.FEI 3017428856Valid toRenews annually
Form 25 / 28
Manufacturing & product licence, State Licensing Authority
Licence no.MFG/MH/2231Valid to31 Dec 2028
How to verify us.
Request
Send the scope of your audit and the standards you work to.
Document review
Licences, site master file and the quality manual, in advance.
Site visit
Production, warehouse, QC laboratory and retained samples.
Written report
Findings answered in writing with a dated corrective plan.
Questions the record cannot answer?
Ask quality directly. A named person replies.
Ask quality