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1. Quality Management in the Drug Industry – 2. ICH Guidelines – 3. Quality by Design – 4. ISO 9000 and ISO 14000 – 5. National Accreditation Board for Testing and Calibration Laboratories (NABL) – 6. Organization, Personnel and Premises – 7. Equipment and Raw Materials – 8. Quality Control Tests for Packaging Materials – 9. Good Laboratory Practices (GLPs) – 10. Complaints – 11. Document Maintenance in the Pharmaceutical Industry – 12. Calibration and Validation – 13. Annexure I to Annexure XIV – Bibliography
ASIN : B084LF967C
Publisher : Nirali Prakashan; First Edition (31 December 2019)
Item Weight : 260 g
Dimensions : 2 x 21 x 18 cm
Country of Origin : India
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