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Quality Assurance

The Responsibilities of QA department concern:

  1. Application and observance of the GMP principles throughout the process, by all the Departments
  2. Monitoring of the quality system performance by annual quality plan, continual improvement
  3. Implementation and updating of SOPs’ system
  4. Implementation and updating of Validation plan, in collaboration with the concerned Technical Departments
  5. Deviations, OOS, Changes, Complaints and CAPA management
  6. Review of Batch Records
  7. Planning and execution of Self-inspections. Assistance to Customers and Regulatory Agencies inspections
  8. Training Programs
  9. Qualifications/Audit of suppliers
  10. Annual Product Quality Review (APQR)
  11. Check and approval of Master Manufacturing Documents and Analytical Methods
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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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