A Guide to GMP Regulations Part 2: GMP Personnel and Documentation - Recorded Webinar
: 4 May 2022 - 31 May 2022
Sector : Pharmaceutical
Type : Recorded Webinar
EudraLex Volume 4 and the CFR Title 21 provide strict guidelines of Good Manufacturing Practice (GMP) which they expect manufacturers to adhere to for consistency of product. Part of these guidelines refer to documentation of processes and responsibilities around areas associated with manufacture, quality control and release of products.
But what are the key roles in a manufacturing unit? Where does ALCOA+ fit in with your documentation? Watch our 15-minute webinar on demand to find out exactly what GMP guidelines require of personnel and documentation in your facility.