- email:registrations@informa-ls.com
- phone:+44(0)20 7017 7481
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QbD for Pharma
24 - 25 May 2011
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QbD for Pharma 2011
Don't miss this opportunity to hear from 3 European Regulators and 10 industry case studies
As PAT and QbD have matured, the pharmaceutical industry has progressed with it’s implementation of these concepts and technological advancements. Informa’s 2011 QbD for Pharma conference will be focused on where and how industry has matured with it’s implementation of QbD and PAT as well as looking at what the future holds.
Although the pharmaceutical industry is now investing more heavily in PAT and working towards full implementation and QbD, management buy-in remains an obstacle for many. QbD for Pharma 2011’s case studies will not only look at the practical implementation, but business decisions behind the real life examples.
Delegates will learn how to improve process understanding and control, and how this will lead to the promised benefits and ROI of PAT and QbD.
2010 Conference Highlights
Homepage speakers
Homepage speakers
Jutta Riedl
Head Quality Review
Swissmedic
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Jobst Limberg
Scientific Director, Head of Unit Cardiology in the Licensing Division
BfArM
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Michael Hahn
QbD specialist
NNE Pharmaplan
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Mette Kraemer Hansen
Quality Risk Management Manager
Novo Nordisk A/S
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Tom Sam
Head Pharmaceutical CMC
Merck Sharp & Dohme
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Stefan Steigmiller
Head of BTS-PMT-PAT-Biotechnology Projects
Bayer Technology Services GmbH
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Jacques Wiss
Head, CHAD PAT Network
Novartis Pharma AG
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Martin Owen
Quality by Design Leader
GlaxoSmithKline
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Spotlight Presentation Sponsor
Media Partners
Pre-Conference Workshop & Evening Seminar
Pre-conference workshop:
Applying QbD Principles - From Development, Registration and Beyond
Evening Seminar:
Use of Statistical Process Control (SPC) in a Pharmaceutical Environment
Reviews
"This conference gave an essential overview of QbD and PAT tools from API derivation to manufacturing of DP and the implementation in various companies"
"Great diversity; regulatory, scientific, financial, chemical, pharmaceutical. A complete overview of QbD/PAT"
"Very useful, informative and will help further information gathering in this area"
Who Should Attend?
Who can I expect to meet?
This leading industry forum is aimed at Directors, Heads of Department, Team Leaders and Scientists working in the areas of:
• Research and Development • PAT • QbD • Compliance
• Process Development & Optimisation • Manufacturing • Formulation
• Quality Assurance/Quality Control • Operations • Regulatory Affairs
• Engineering • Process Science • Process Analytics
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Dates and Venues
24 May 2011 - 25 May 2011
Maritim Hotel Berlin
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