Cherwell, specialists in cleanroom microbiology solutions for the pharmaceutical, healthcare and related industries, has published an update to its guide on “Environmental Monitoring Processes and Validation”, incorporating specific detail on the new version of EU GMP Annex 1. This aims to help…

Arbeiten Sie nach dem Annex 1 und fragen Sie sich, was für Auswirkungen der neu veröffentlichte Leitfaden für ihr Monitoring-System hat?

Briem hat sich intensiv mit dem Update auseinandergesetzt und wird in seinem kompakten LIVE-Webinar über die wichtigsten Neuerungen informieren.

Die Briem-Experten Sasch…

Cherwell Laboratories, specialists in cleanroom microbiology solutions for the pharmaceutical, healthcare and related industries, will be leading an open discussion on environmental monitoring (EM) in line with EU GMP Annex 1 at the forthcoming Pharmig 30th Annual Conference. The annual event to be…

Introduction

On December 20th, after intensive research and debates, the draft for a Revision of ANNEX 1 ("Manufacture of Sterile Medicinal Products") of the EU Guideline for GOOD MANUFACTURING PRACTICE for drug products and drug substances was published for public comment. This updated document will…