Quality
Certified, audited, verifiable.
The documentation a procurement team checks before the first enquiry — kept current and shared on request.
WHO-GMPWHO Good Manufacturing Practices
ISO 9001Quality Management System
ISO 14001Environmental Management System
SGSSGS third-party inspection
IntertekIntertek testing & certification
BISBureau of Indian Standards
FIEOFederation of Indian Export Organisations
IECImporter-Exporter Code (DGFT)
From raw material to release
1
Incoming inspection
Every raw material is identity-tested and released before it enters production.
2
In-process control
Reaction monitoring and intermediate checks keep each batch on specification.
3
Finished-goods release
Full analysis against the agreed spec; a certificate of analysis accompanies every batch.
4
Retention & stability
Retention samples on every batch; stability studies support shelf-life and storage claims.
pharmachem-04b-lab-altDocumentation
The paperwork that clears customs.
- Certificate of Analysis (COA) per batch
- Material Safety Data Sheet (MSDS / SDS)
- Drug Master File (DMF) support on regulated lines
- BSE/TSE, allergen and origin declarations
- Stability data and method validation on request