Webinar, Online
A unique opportunity to attend a short and insightful webinar led by one of the Pharmaceutical Industry leaders, GSK.
Overview
Does the prospect of Validation make you feel like you’re under threat?
Validation and Qualification expectations continue to develop and change, with the regulatory bar becoming increasingly elevated standards need to be high, and the resulting documentation is ever popular with regulatory inspectors.
But ‘Taming the beast’ is possible and can lend real value to making pharmaceuticals.
Join this webinar for a short and detailed tour through some practical approaches and techniques that experience has shown can make a real and positive difference when approaching these fundamental activities and can offer some food for thought along the way.
Register your place for this free webinar today!
Day 1
12:00 - Webinar Programme
12:00 GMT WEBINAR BEGINS
12:30 GMT Q&A BEGINS
13:00 GMT WEBINAR ENDS
Karen Stevenson: Compliance Officer, GlaxoSmithKline
Karen Stevenson has worked in the Pharmaceutical Industry for over 2 decades across Quality GxP and automated systems auditing, Validation, Regulatory Affairs and Engineering; covering a range of dosage forms, Oral to Sterile. Ms Stevenson’s current role is in Compliance, working for GSK’s Global Manufacturing and Supply, Engineering and EHS global support function.
Focusing on Validation for over 15 years, from engineer to Senior Management, Karen has plenty of practical experience to draw on, having worked across a wide range of equipment, utilities, automated and computer systems and manufacturing process. Having spent many hours in conversation with regulatory inspectors when they came to call means she understands well the importance of a robust validation approach.
Karen is Chair of the Pharmaceutical Technical Activities committee of the Institution of Mechanical Engineers (London)
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