'Action limits' diaporamas de présentation

Production and Process validation

Production and Process validation. 17 January 2006. by...Wiriya charoenkunathum. References:. GMP for pharmaceutical products: main principles ; WHO TRS No. 908,2003 GMP for biological products ; WHO TRS No.822,1992 A WHO guide to GMP requirements, part 2:validation ; WHO,1997. GMP.

1.9k views • 60 slides

Control Charts

707 views • 40 slides

Impurity Monitoring in a Pharmaceutical Process

Impurity Monitoring in a Pharmaceutical Process. Dr Elaine Martin and Professor Julian Morris Centre for Process Analytics and Control Technology (CPACT) University of Newcastle. Overview of Presentation. Initial Analysis of Data from a Drug Intermediate Objectives Process Description

614 views • 33 slides

Transfer Disinfection Validation

Transfer Disinfection Validation. Sarah Hiom Cardiff and Vale NHS Trust. Aseptic Preparation Isolator Technology. Transfer into controlled work zone. ? High contamination risk ? Disinfection (70% alcohol). Validation of Disinfection Transfer. Current methods Swabs/Contact plates

370 views • 21 slides