Clinical Evaluations & Investigations for Medical Devices 2014

Key Topics

• Successfully adapting to changing regulatory requirements
• The impact of the revision of the Medical Devices Directive (MDD) on clinical evaluations and investigations
• How the revision of the Data Protection Directive will impact clinical investigations and data
• Regulations changes over the past two years and further changes expected
• Deciding which country to carry out your clinical trial and which authorities will be involved
• How to prepare for the revision of the Data Protection Directive and remain compliant
• The implications of the MDD revision on setting up post-market clinical follow-up
• Practically conducting clinical investigations in emerging market regions

Who should Attend

• Clinical research
• Clinical project manager
• Clinical affairs
• Clinical operations
• Clinical Program Manager
• Regulatory affairs
• Quality Manager
• Clinical Project Leader
• Postmarket Surveillance