Testing of Materials in Pharmaceuticals (Good Manufacturing Practices GMP in warehouse) Part II

This training session will make you understand about testing, approval and rejection requirements as 21 CFR part 211. Means as per FDA expectations. I have made the requirements in easy to understand and simple language.

[@raheemkhan4083]

Thanks sir

[@hitendrakumarshah3718]

Raheem Khan welcome. Please keep learning!!!

[@proogamerop5266]

Very good learning sir

[@hitendrakumarshah3718]

Thanks you. Keep Learning !!!

[@abdulrehmanshaikh6933]

Dear Sir, can we instruct retest raw materials only before use, no need to test as per the frequency such as six month or annually....

[@hitendrakumarshah3718]

Yes. But, the retesting date should not cross the material expiry date or retest date assigned by supplier.

[@navindoshi2826]

Dear Sir , Pls guide on use of retest material after 5 years even & if raw material label of manufacturers shows expiry then can use if passes in retest or user trial ? Thanks in advance

[@hitendrakumarshah3718]

you need to check with vendor whether they are having extended shelf life stability study or not? I suggest you can go through the Q&A session of below webinar. You will get more clarity on this. czcams.com/video/lQUUP8hEILA/video.html

[@deepakdhiman1417]

Dear sir
Please guide us to reduce testing of raw materials.

[@hitendrakumarshah3718]

Sure. Will arrange discussion/training on reduced testing.