Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
1. Overview of health industry India and global perspective...(past and present and likely future)
2. Role of regulatory body ...
3. Role of IDMA
4. Good Manufacturing Practice (GMP)...
5. What is QC, QA...
6. Importance of Compliance management
7. TQM - Need of the hour...
8. What are the departments supports TQM...
9. Purchase, lab test, production, post manufacturing bio availability test..
10. API and exciepients - value addition for TQM...
11. WHO and GMP guide lines and certification...
12. Factory inspection, Maintenance, zero bacteria zone, log book Maintenance...
13. Batch size and expiry as per the guidelines...
14. Preservatives...
15. Tablet coting...
16. Nutritional supplements both veg and non veg source...marking, gelatine and soft gel and capaules...
17. Tablet coating as per IP, USP and BP grade...
18. role of IPA, MDC (Methaline Choride) both commercial and LR grade uses as per standards.
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
Students undergoing B Sc Chemistry and related subjects would be undergoing Vocational course. The faculty from Department of Chemistry would be undergoing Faculty Development Program. .
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
GMP covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff. Detailed written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made.
GMP certification ensures that hygiene and cleanliness requirements are maintained throughout the manufacturing and logistics chain. This includes implementing practices to prevent contamination and ensure product safety.