The Environmental Monitoring Processes and Validation Guide

This eBook was created following the release of the revised draft of EU GMP Annex 1 – Manufacture of Sterile Medicinal Products. We’ve addressed and summarised the key changes proposed to the EU GMP Annex 1, so you remain completely informed. We’ve put together some suggestions of environmental monitoring best practice and practical steps to implement an effective EM program. In this guide you will find insight into: Why the EU GMP Annex 1 draft has been proposed How it helps all industries move closer towards a global standard The main changes found in the draft revision How to prepare for compliance Examples of best practice of EM programs The right tools needed for an effective and compliant program Please complete the form on the right to receive your copy. Once you have submitted the form, we will send you your copy by email. P.S. We will keep all your details private in line with our privacy policy.

For more information on The Environmental Monitoring Processes and Validation Guide talk to Cherwell Laboratories Ltd