Tablet Process Development and Validation and the application of QbD (2 day)

Venue: Window Conference Venue

Location: London, N1 8QG, United Kingdom

Event Date/Time: Nov 28, 2011 End Date/Time: Nov 29, 2011
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This interactive workshop provides up-to-date, relevant and detailed information on the impact of Quality by Design (QbD) on the Development and Validation of tablet manufacturing processes. It will also study the identification and evaluation of Critical Product Attributes and Critical Process Parameters for tablets, and their implications for process control. We develop new concepts including the use of risk and process matrices for risk management. The latest ICH and FDA guidance on Quality by Design and Process Development, published in 2009, will be comprehensively reviewed.

Who should attend:
Tablet formulation and process development staff and those involved in managing process development and validation, and commissioning products into production. Regulatory Affairs staff preparing dossiers for tablet products. Quality Assurance personnel responsible for the design or implementation of tablet process validation protocols.


13 Windsor Street, Islington
United Kingdom