Téléversements by qac gmp

The History & Future of Validation

ISPE Good Practice Guide and Compressed Air

Performance and improvement of cleanroom environment control system related to cold-heat offset in clean semiconductor fabs

Cleanroom process model

BS ISO 14644‑122018 by The British Standards Institution

“GANTT CHARTS FOR PRODUCTION FLOW” FRAMEWORK

‘Quality by Design’ approach for the analysis of impurities in pharmaceutical drug products and drug substances

Automating MACO Calculations in Cleaning Validation

A Science and Risk-Based Pragmatic Methodology for Blend and Content Uniformity Assessment

Setting Cleaning Validation Acceptance Limits for Topical Formulations

Extensions to the ICH Q1E Approach for the Statistical Evaluation of Stability Data for a Large Number of Lots

Statistical Tools for Development and Control of Pharmaceutical Processes_ Statistics in the FDA Process Validation Guidance