Drugs, Devices and Regulations '07

This event will address the Agency’s regulatory processes for approving medicines and medical devices. It will focus on delegates learning about best practices and the latest in regulations governing those practices. Topic areas such as the law, regulations and

policies associated with approving medicines and medical devices, as well as providing ‘real life’ case studies will be explored. The various regulatory processes will also be presented, including the major inspection and enforcement activities of the Agency.

This event aims to provide a unique opportunity for healthcare professionals, industry and the patient representatives to share knowledge and exchange information in how we all work towards safeguarding public health.

Target Audience
DDR 07 attracts over 750 delegates from around the world and offers sponsors and exhibitors access to an audience of leading healthcare professionals. These include:

• Regulatory affair managers
• Clinical research professionals
• Healthcare professionals
• Device manufacturers
• Patient Groups
• NHS Managers
• Clinical Investigators
• R&D Managers
• Drug Safety personnel
• Pharmaceutical physicians
• Clinical Directors
• Patient Safety professionals
• Research Scientists
• Senior Executives
• Contract manufacturers
• CEOs

Event Fee:
Private Sector: 2 days - £1050, 1 day - £575

Early Bird Booking rate (book before 30th September 2006): 2 days - £840, 1 day - £460

Public Sector: 2 days - £575, 1 day - £375

Early Bird Booking rate (book before 30th September 2006): 2 days - £460
1 day - £300

Registration and more Information
To register or for more information on the conference please visit http://www.ddr07.co.uk/

Or contact:

E: mhraconferences@mhra.gsi.gov.uk
T: +44 20 7084 2903
F: +44 20 7084 3522
W: www.mhra.gov.uk/conferences