QA

Quality Assurance

Believing in a strong principle rule “Do what you write and write what u do”, the QA department of OPL monitors the overall aspects of pharmaceutical industry. The department is committed to vouch the integrity of products to meet the standard for the proposed use. The intellectual, accomplished and experienced staffs in the department continue to work in order to develop a systematic approach for the production of quality products. 

The main functions of QA department involve: 

1. Establish the quality system

2. Development of Quality Policy

3. Establish procedures and specifications

4. Review and approve or reject all things CGMP

5. Controlled Documentation and Record keeping

6. Preparation of BMR.

7. Batch or Lot Disposition

8. Internal Audit

9. Change control

10. Problem investigation

11. Customer compliance

12. Annual product review

13. Environmental monitoring and control

14. Effective communication to all departments

15. Validation of process, equipment, facility, cleaning and analytical tests.

16. Making recall decision

17. Keeping the management informed

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