Webinar Overview
Whether you’re based in Europe, North America, Japan, or Brazil a change is afoot in terms of how bioanalytical validation and sample analysis is undertaken as we move from many regional sets of bioanalytical guidelines to a single harmonized document – The ICH M10 Bioanalytical Validation Guideline.
This guideline was finalized on 24 July 2022 and will shortly be adopted by regulatory authorities around the world.
During this webinar, you will gain a deeper understanding of the changes within this new internationally harmonized bioanalytical guideline, including:
- The field of bioanalysis
- The bioanalytical guideline ICH M10
- The core difference between previous EMA/FDA guidelines and the new ICH M10 guideline
Webinar Presenters
Hannah Mather, BSc
Study Director, Department of Chromatographic Bioanalysis
Charles River
Iain Love, BSc
Director, Chromatographic Bioanalysis & Residues
Charles River
Additional Information
- Nonclinical and Clinical Bioanalysis
- Drug Metabolism and Pharmacokinetics
- Method Development and Validation
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