Analytical & Stability
The activities of the QC Department
- Vendor evaluation
- RM and PM Testing As Per pharmacopieal Standards.
- Creating In-house standard where necessary
- In process QC
- Finished Product QC
- Random Testing
- Development and validation of analytical methods for RM / PM / Finished products
- Accelerated and real time stability studies.
We have full-fledged Quality Control Laboratories with separate areas for Chemical, Instrument, Microbiology and Package testing. Our laboratories are well equipped with sophisticated instruments like HPLC, FTIR, Dissolution testers, UV-Visible spectrophotometers, Humidity chamber and LAF units. These instruments are calibrated periodically to check their performance so as to avoid any manual errors.
Our Quality Control and Assurance team consists of highly experienced and qualified personnel having expertise in various disciplines like Chemistry, Microbiology, Pharmacy and other relevant areas.
Every raw/packaging material received at the manufacturing sites is procured only from well-established and approved manufacturers or suppliers. Approved vendors are judged by a vendor audit or by evaluating their yearly performance.
Each raw/packaging material is sampled and analysed by Q.C. before releasing for production. Additional tests like solubility, water content, chromatographic purity and particle size are done on ingredient to ensure highest quality.
Finished products are analysed as per pharmacopieal specification and additional stringent in-house specifications.