Tablet Process Development and Validation and the application of QbD
Venue: Window Conference Venue
|Event Date/Time: Dec 16, 2010||End Date/Time: Dec 17, 2010|
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.
By the end of the course, you will
* Understand the relationship between the principles of QbD and tablet development and process validation in generic and new product development
* Understand the relationship between material properties, formulation development and process development
* Understand the processes commonly used to manufacture tablets and the factors which affect them
* Recognise how to identify critical processing parameters, and how to incorporate into a process validation program
* Understand the principles of PAT, how and where it can be most effectively deployed
* Know the latest FDA thinking on Process Development including the three key steps of validation
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. Numbers will be limited to give participants the opportunity for thorough discussion of the issues to be covered by the programme and one on one consultation with speakers.