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Introduction

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

Downloads

• Tablet-Process-Development-Validation-QbD1.pdf

Venue

CCIT, The Technology Centre of New Jersey

CCIT, The Technology Centre of New Jersey, 675 US Highway One, North Brunswick, 08902, United States

Useful links

Organised by

PharmaTraining Ltd

Contact information

Mrs Judy Callanan
BioCity, Pennyfoot Street, BioCity, Nottingham, NG1 1GF, United Kingdom
442071937703
Contact us by email

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