QbD & PAT - The Scientist Is No Longer In The Laboratory, But Integrated In The Overall Quality Process
Date: 4th October 2012
Time: 3PM London / 10AM New York
Duration: 60 Minutes

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Sponsored By:
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Join this 1hr FREE Webinar: Economic Pressures to Reduce Effort on Compliance and Improve Quality have Accelerated the Adoption of Quality by Design and PAT


The industry is looking at more holistic approaches to improve processes of bringing new products to market that can accelerate product development and lower operational costs. Quality by Design (QbD) has come relatively late to the pharmaceutical industry. In terms of quantifiable benefits, the main QbD value comes from four main areas; (1) a reduction of Cost of Goods Sold (COGS) and capital expense, (2) increased technical development productivity, (3) improved quality and lower risk, and (4) increased sales.

This webinar explores the journey and its role in driving QbD and Pat adoption within Pharma and gives answers of some of the concepts behind the QbD concept. Join now to be part of this interesting webinar session and to be part of the LIVE Q&A. Read More


Speaker Synopsis

Peter J. Boogaard,
Director
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Key Learnings
  • Introduction to QbD concept and update on ICH Q10 and QbD Pharmaceutical Quality Systems guideline
  • Overview of PAT technologies and industry examples in both development and manufacturing
  • Introductory overview of Product Quality Lifecycle Implementation (PQLI) and Introduction to the 4 Product Quality System elements (PQS)
  • Introduction to paperless lab initiative, to help you eliminate the informatics information silo’s

We look forward to your attendance at this event. If you require any further information regarding this webinar, please contact us.

Kiki Newell
Tel: +44 (0)207 936 6978
Email: [email protected]


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