The QA is responsible for preserving whole quality system and achieving current GMP standards. The QA department has been established for the aim of designing and implementing a well-developed pharmaceutical quality system and therefore improving products quality in accordance with cGMP.
The roles and responsibilities of QA department cover the following points:
* Documentation
* Validation
* Conducting Audits
* Regulatory affairs
The QA department monitors following affairs in the company:
* Quality Manual
* Documented Procedures (SOPs)
* Self-Inspection and Foreign Inspection
* Distributors and Sellers Evaluation
* Product Release
* Personnel Training
* Change Control and IPC
* Calibration
* Complains and Recalls
* Suppliers Evaluation