Presented By:
Tony Harrison - Senior Marketing Manager, Beckman Coulter
Speaker Biography:
Tony held the Convenorship of the ISO Working Group revising ISO 14698-1 & -2 for microbial control in cleanrooms and was the UK subject matter expert to the ISO Working Group who issued the 2015 revised versions of the ISO 14644-1 & -2 documents for cleanroom classification at the heart of the aseptic manufacturing chapters of both the European GMP and the USA cGMP documents.
Webinar:
Validating a Pharmaceutical Total Organic Carbon Benchtop Analyser to ICH Q2
Webinar Abstract:
The International Committee for Harmonisation issued their recommendations on validating an analytical instrument, ICH Q2, to support users of analytical equipment such as Total Organic Carbon (TOC) analysers. It covers all the important aspects of validating an analyser, including ensuring that it is suitable for the test conditions of the application and the random effects on intermediate precision caused when different technicians perform the same test, i.e. human error. This webinar explains the different aspects of ICH Q2 and how they apply to TOC analysers used in pharmaceutical applications.
Learning Objectives:
-Summarize how to interpret ICH Q2 for TOC analysers
-Identify how to demonstrate compliance to ICH Q2 for TOC analysers
-Explain the opportunities to improve TOC analysis data integrity in your QC laboratory
Earn PACE Credits:
1. Make sure you’re a registered member of LabRoots ([ Ссылка ])
2. Watch the webinar on YouTube or on the LabRoots Website ([ Ссылка ])
3. Click Here to get your PACE credits (Expiration date – November 05, 2021 08:00 AM): [ Ссылка ]
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