REGULATORY AFFAIRS
FOR SUPPORT STAFF ~
PART 1

Conference Date: 12 Oct 2009
Conference Ref: P10-4109
Fee: £510 + VAT
Venue: The Rembrandt Hotel, London

Two days of training which can be booked individually or together. Discount available if both courses booked

Topics to be covered:

• Learn about the Drug Development Process – from Drug Discovery to Product Launch and Beyond
• Understand the background of European Law – Regulations, Directives, etc.
• Discover where you can find information on Regulatory Affairs, Approvals, Withdrawals, etc.
• What is the Centralised Procedure?
• Understand the EU Clinical Trial Directive
• How to Seek Scientific Advice in Europe
• What is the Common Technical Document

With: Ryta Kuzel Director, European Regulatory Affairs, Johnson & Johnson Pharmaceutical R&D, UK

Click here to book your place on this important event.