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ICH M10 Bioanalytical Method Validation Guideline-1 year Later
by
Yu, Chongwoo
, Wickremsinhe, Enaksha
, Vazvaei-Smith, Faye
, Woolf, Eric
in
Biochemistry
/ Biological Availability
/ Biomedical and Life Sciences
/ Biomedicine
/ Biotechnology
/ Drug Stability
/ Guidelines as Topic
/ Humans
/ Meeting Report
/ Pharmaceutical Preparations - analysis
/ Pharmaceutical Preparations - standards
/ Pharmacology/Toxicology
/ Pharmacy
/ Quality Control
/ Validation Studies as Topic
2024
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ICH M10 Bioanalytical Method Validation Guideline-1 year Later
by
Yu, Chongwoo
, Wickremsinhe, Enaksha
, Vazvaei-Smith, Faye
, Woolf, Eric
in
Biochemistry
/ Biological Availability
/ Biomedical and Life Sciences
/ Biomedicine
/ Biotechnology
/ Drug Stability
/ Guidelines as Topic
/ Humans
/ Meeting Report
/ Pharmaceutical Preparations - analysis
/ Pharmaceutical Preparations - standards
/ Pharmacology/Toxicology
/ Pharmacy
/ Quality Control
/ Validation Studies as Topic
2024
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Do you wish to request the book?
ICH M10 Bioanalytical Method Validation Guideline-1 year Later
by
Yu, Chongwoo
, Wickremsinhe, Enaksha
, Vazvaei-Smith, Faye
, Woolf, Eric
in
Biochemistry
/ Biological Availability
/ Biomedical and Life Sciences
/ Biomedicine
/ Biotechnology
/ Drug Stability
/ Guidelines as Topic
/ Humans
/ Meeting Report
/ Pharmaceutical Preparations - analysis
/ Pharmaceutical Preparations - standards
/ Pharmacology/Toxicology
/ Pharmacy
/ Quality Control
/ Validation Studies as Topic
2024
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ICH M10 Bioanalytical Method Validation Guideline-1 year Later
Journal Article
ICH M10 Bioanalytical Method Validation Guideline-1 year Later
2024
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Overview
The International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) adopted Guideline M10 entitled \"Bioanalytical Method Validation and Study Sample Analysis\" in May 2022. In October 2023, approximately one year after the adoption of the ICH M10 guideline, a \"Hot Topic\" session was held during the AAPS PharmSci 360 meeting to discuss the implementation of the guideline. The session focused on items the bioanalytical community felt were challenging to implement or ambiguous within the guideline. These topics included cross-validation, parallelism, comparative bioavailability studies, combination drug stability, endogenous analyte bioanalysis, and dilution QCs. In addition, the regulatory perspective on the guideline was presented. This report provides a summary of the Hot Topic session.
Graphical Abstract
Publisher
Springer International Publishing,Springer
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