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Quality Assurance

QA responsibilities:

1. Maintaining the compliance of the Pharmaceutical Quality System (PQS) to the cGMP and applicable regulations
2. Monitoring and promoting improvements of the PQS
3. Managing Self audits
4. Managing Deviations/Investigations and implementing CAPA system
5. SOP management
6. Management of the master manufacturing document
7. Participate and supervises the activities concerned with the validation of manufacturing processes, equipment, analytical methods and computerized systems
8. Approval of the reference documents for analytical methods
9. Handling quality complaints and investigation
7. GMP Training
8. Review of the batch records
9. Annual Product Quality Review (AQR)
10. Change Control system
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Valpharma S.p.A. - Via Ranco, 112 - 47899 - Serravalle - Tel. +378 0549 900936 - E-mail: valpharma@valpharma.com- Privacy Policy - C.o.E. SM02686
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