Fortis Life Sciences
 
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A Guide to GMP Regulations – Part 4: Minimising Contamination

: 13 Sep 2022 - 12 Oct 2022

Sector : Pharmaceutical

Type : Webinar, Recorded Webinar, Prerecorded Webinar


This is the final part of our GMP mini series. Catch up on Part 1, Part 2 or Part 3.

Do you know what GMP guidance such as EudraLex Volume 4 and the CFR Title 21 say about minimising contamination in your final drug product?

What's required of you
Find out what's required according to EudraLex Volume 4 and CFR Title 21 to minimise contamination,

Microbiological environmental monitoring
How you identify potential routes of contamination, and keep an eye on the state of your cleanroom.

What to do with all of your data
How you can use your data to make better decisions in your facility.

Click here to  register or use the Request Information button below. 

Venue

Online event


Organizer

Microgenetics


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Air Monitoring Facil...
Next article > >
Faster Micro QC Rele...