| Incorporating Quality by Design (QbD) in the analytical research, product development, manufacturing processes and regulations implementation is becoming an increasingly critical component for generic pharmaceutical companies. |
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| Attend Pharma Quality by Design 2012, a 2-day exclusive business conference to gain in-depth insights into: |
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- QbD overview and what’s in it for pharma companies?
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Complete regulatory evaluation process and implementation path as per FDA requirements
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Role of QbD in analytical method development and validation
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Cost-effective strategies to implement PAT
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ICH Q11 requirements and their impact on API development
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Role of excipients in QbD
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Elements of QbD and challenges in product development
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Case studies on conventional and complex formulations
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| PLUS! DOE for QbD Workshop:
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| A must-attend interactive workshop to help delegates get to grips with the Design of Experiments (DOE) including the basics of statistics, factorial design and QbD with comprehensive and illustrative examples |
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| Event Highlights: |
- Hands-on workshop – Gain in-depth understanding on the DOE aspects of QbD with the help of illustrative and comprehensive examples
- Extended Q&A sessions – Come armed with your most challenging questions and leave with a toolkit of practically implementable solutions pertaining to effective implementation of QbD at each product development stage
- Speed networking – Meet a wide variety of people in quick succession and strike-up profitable relationships…. bring plenty of business cards!
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| With a comprehensive agenda, Pharma Quality by Design 2012 brings you an unparalleled information interface and networking platform, helping you to get an edge in the fast developing Indian pharmaceutical market. |
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| Gold Partner |
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| Media Partners |
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