Good Storage Practices for Pharmaceuticals
This course will take you thoroughly to understand about Good Manufacturing Practices with special focus on warehouse.
Description
Most of all regulatory inspections starts with Warehouse/storage facilities. To ensure first good impression and long lasting impression, it is very important to pay compliance attention to this area. Also, as a part of basic GMP(Good Manufacturing Practices) training requirement, all the persons working in the area should be trained on GMP. So, this session will help you all to get trained about good warehouse practices followed by certification from Udemy.
With this training session, you will learn about difference between Good Manufacturing Practices and BEST Manufacturing Practices. Further short learning videos and detailed lecture on good warehouse practices. These lectures are made on the basis of requirements of FDA, EUGMP,WHO, ANVISA, PIC/S,TGA &Schedule-M.
This training session will specially focus on all aspects about warehouse. For example, receipt of materials, storage of materials, issuance of materials, reconciliation of materials and many more. Furthermore, wherever required, specifics for printing packing materials, primary packing materials, active materials and inactive materials is discussed.
The good warehouse practices session 2 will specifically covers Brief recap on session-1 of this subject,Sampling & Testing requirements,Precautions during sampling and testing,Retesting requirements,Requirements for weighing areas, Finished product handling, Dispatch and Transportation, Brief about Recall and Return goods.
If you have any questions, please feel free to put in comment section. I will revert with your all queries.
What You Will Learn!
- This course has been created for all pharmaceutial professionals to learn Good Manufacturing Practices with special focus on Warehouse or Storage areas in Pharmaceuticals
Who Should Attend!
- Pharmacy students, Pharmaceutical professionals, consultants etc. This course is essential for auditors, quality staff involved in GxP applications. • Regulatory Affairs • QA/ QC • IT/IS • Software Managers • Project Managers • Software vendors and suppliers