Pharma QbD 2012

A must-attend event for analytical, formulations, manufacturing and regulatory heads to learn practical approaches to pharmaceutical QbD!

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.

Attend Pharma Quality by Design 2012, a 2-day exclusive business conference to gain in-depth insights into:

•QbD overview and what’s in it for pharma companies?
• Complete regulatory evaluation process and implementation path as per FDA requirements
• Role of QbD in analytical method development and validation
• Cost-effective strategies to implement PAT
• ICH Q11 requirements and their impact on API development
• Role of excipients in QbD
• Elements of QbD and challenges in product development
• Case studies on conventional and complex formulations

PLUS!
DOE for QbD Workshop:

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

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!