11-13 October 2010
Lisbon, Portugal

The DIA 4th Annual Clinical Forum provides access to sessions covering nine multidisciplinary themes, including Clinical Data Management/eClinical, Clinical Operations, Clinical Research, Peri- and Post Approval Studies, Drug Safety and Risk Management, Quality Assurance, Clinical Endpoints, e-Technology and Validation and Medical Information & Communications.

WHO SHOULD ATTEND

Pharmaceutical and Biotech Industry Professionals from Academia, CROs, Clinical Trial Sites, SMOs, Health Regulatory Agencies and Patient Organisations

Areas of interest include:

• Clinical Data Management/eClinical
• Clinical Operations, Clinical Research, Clinical Safety and Pharmacovigilance
• Quality Assurance
• Clinical Study Endpoints
• Statistics, Project Management, Medical Affairs
• Non Interventional Studies
• Business and IT Computer System Validation
• Medical Information, Medical Communications

Click here for more information or to register online.

Exhibit at the Clinical Forum 2010

The DIA provides you with the opportunity to interact with a truly global audience of qualified professionals, from entry level to expert, in the biopharmaceutical industry, contract service organisations, regulatory agencies, health ministries, patients, universities and students throughout Europe and worldwide.

For more information, please contact Natacha Scholl at +41 61 225 5159 or Natacha.Scholl@diaeurope.org.

For more information on the Clinical Forum, please contact the Customer Services Team on +41 61 225 5151, or email: diaeurope@diaeurope.org

We look forward to welcoming you to Lisbon in October!