Quality assurance

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

 

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