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One might easily get the impression that the GMP world is continuously turning faster. Laws, regulations, and especially GMP requirements worldwide are constantly renewed, modernized and adapted against each other. To provide you with an overview what is going on in the area of microbiology and hygiene is thus the goal of this webinar.
This webinar aims at giving you a comprehensive but still compact overview about the many innovations in the GMP area of microbiology and hygiene - those already realized and those planned:
EU and US Directives and EU-GMP Guide
EU and US Pharmacopeial Chapters
News from FDA and other Agencies
Outlook what is coming up
The webinar targets executives and staff of pharmaceutical microbiological laboratories and contract laboratories as well as responsible regulators and inspectors. Additionally, it will be of interest for responsible persons from QC and QA who must evaluate and estimate microbiological data.
Dr Marcel Goverde, MGP Consulting
Mr Goverde holds a PhD in Biology and runs since 2011 his own company for consulting, training and project management in GMP-relevant areas with focus on microbiology, hygiene and deviation management. He gathered 8 years of work experience in microbiological pharmaceutical industry at F. Hoffmann-La Roche Ltd and another year as QC expert for microbiology at Novartis Pharma. Since 2003 Mr. Goverde acts as a Swiss delegate in the EDQM group for microbiological and statistical methods and since 2011 as board member and deputy chair of the ECA Pharmaceutical Microbiology Working Group. He is a regular speaker at different institutions.