Transcription of Draft Guideline on Bioanalytical Method Validation …
{{id}} {{{paragraph}}}
Draft Guideline on Bioanalytical Method Validation in pharmaceutical development 15 April 2013, MHLW, Japan) 2 Table of Contents 1. Introduction 2. Scope 3. Reference Standard 4. Analytical Method Validation Full Validation Selectivity Lower limit of quantification Calibration curve Accuracy and precision Matrix effect Recovery Carry-over Dilution integrity Stability Partial Validation Cross Validation 5. Analysis of Study Samples Validity and reproducibility of analytical Method in analysis of study samples Calibration curve QC samples Incurred samples reanalysis (ISR) Carry-over Points to note Calibration range Reanalysis Chromatogram Integration System suitability 6. Documentation and Archives List of Relevant Guidelines Glossary Annex 3 1.
Draft Guideline on Bioanalytical Method Validation in Pharmaceutical Development (15 April 2013, MHLW, Japan)
Domain:
Source:
Link to this page:
Please notify us if you found a problem with this document:
{{id}} {{{paragraph}}}
Chapter-2 Analytical Method Development and, Chapter-2 Analytical Method Development and Validation, Development, Bioanalytical, Method validation, Validation, Strategic Considerations for ffoorr for Successful, Method, Method Development, Preview - Validation of Analytical Methods for, Guide to Effective Method Development in, GUIDE TO EFFECTIVE METHOD DEVELOPMENT IN BIOANALYSIS, Development and Validation, Up Your Analytical Method Transfer, And “validation