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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
Annexure I to Annexure XIV
Bibliography
| Weight | 260 g |
|---|---|
| Dimensions | 19 × 25 × 2 cm |
| Language | English |
| Publisher | |
| Semester - Year | Semester 6 (Third Year TY) |
| University |
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