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Part 2: GMP Personnel and Documentation

Watch Part 2 in our GMP mini-series. If you need to catch up on Part 1, click here! Alternatively, skip to part 3.

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. Simply fill out the form below!

What you'll discover on this webinar...



From key roles to Quality Units, the importance of your people.



How and why maintenance of documentation is key to quality assurance. 


Paperless EM

How paperless environmental monitoring solves documentation challenges. 

Fill out the form below to watch now!


Ed Webber

Product Specialist, Microgenetics 

Quality professional turned Product Specialist for Microgenetics, Ed will be your presenter for this webinar.

With his background as a QC Manager, he has a deep understanding around the importance of a Contamination Control Strategy and how this is only going to increase with the new Annex 1. 

At Microgenetics, he is the voice of Quality professionals, writing technical articles and ensuring our products will help to solve some of the biggest challenges in environmental monitoring.