Recording Webinar: Microbiology Update
Costs
| ECA-Member: | EUR 199,-- | |
| Non ECA Member: | EUR 249,-- |
(All prices excl. VAT)
If you have any questions, please contact us:
Tel.: +49 (0)6221 / 84 44 0 E-Mail: info@concept-heidelberg.de
Speakers
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
Background
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.
Target Group
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.
Technical Requirements
To be able to take part in a Webinar, you need a computer with high-speed Internet access (i.e. DSL) and speakers.
Your Internet browser must have following features to use the GMP Webinar system:
1. Adobe Flash-Player must be installed.
2. Javascript must be allowed.
3. Port 1935 must be released.
Programme
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
Recording from 07.12.2016
Duration of recording: 1,5 h.
Recorded GMP Online Training/Webinars by topic
- Quality Assurance
- GMP in Biotechnology
- Microbiology
- Regulatory Affairs
- GMP in Pharmaceutical Development
- Quality Control
- GDP - Storage/Distribution/Transportation
- Sterile / Aseptic Manufacturing
- IT / Computer Validation
- Validation
- Technical Operations
- GMP for APIs and Excipients
- Medical Devices/Combination Products
- Basic Training
- Packaging
- Data Integrity