Quality Assurance
Uncompromising quality from molecule to medicine
Quality is the foundation of every INMAAS product. Independent QC, validated processes, and internationally recognised standards ensure every dose we release is safe and effective.
Our QA Process
Six checkpoints, zero shortcuts
Raw Material Inspection
Every incoming raw material is quarantined, sampled, and tested against USP/BP monographs before release.
In-Process Testing
Blend uniformity, weight variation, hardness, and dissolution monitored throughout production.
Analytical Testing
HPLC, UV, dissolution, and microbial testing on every finished batch in our in-house QC lab.
Batch Release
Two-person Quality Assurance review of every batch record before finished-goods release.
Documentation & Traceability
Full electronic batch records — traceable from raw material lot to pharmacy shelf.
Post-Distribution Surveillance
Stability studies, complaint handling, and periodic quality review.
In-House Laboratory
A lab equipped for the tests that matter
Our analytical laboratory is fully equipped to test raw materials, in-process samples, and finished products — with instruments calibrated and validated according to international pharmacopoeial standards.
- High-Performance Liquid Chromatography (HPLC)
- UV-Visible Spectrophotometry
- Dissolution & Disintegration testing
- Microbial Limit & Sterility testing
- Karl Fischer moisture analysis
- Stability chambers (25°C / 40°C)
Need a Certificate of Analysis?
A batch-wise Certificate of Analysis (COA) is available on request for institutional buyers, distributors, and regulators.