CE Marking for Medical Devices Including In Vitro Diagnostic Devices - Webinar By GlobalCompliancePanel 2012

Key Topics

• Overview of European Medical Device Regulations and Regulatory Framework for Medical Devices
• How EU laws are made
• Active Implantable Medical Device Directive (AIMDD)
• Medical Device Directive (MDD)
• The directive amending MDD and AIMDD
• In Vitro Diagnostic Device Directive (IVDD)
• ISO 13485, ISO 14155, and ISO 14971
• CE marking principles
• GHTF and MEDDEV guidance documents

Who should Attend

• Clinical Affairs Managers, Directors and VPs
• Regulatory Affairs Managers, Directors and VPs
• Quality Managers, Directors and VPs
• Quality Managers, Directors and VPs
• Sales and Marketing Managers, Directors, and VPs
• Compliance Managers and Directors
• Site Managers, Directors, and Consultants
• Complaint Handling and Risk Management Managers and Directors
• Compliance Officers and Legal Counsel
• Senior and Executive Management
• Business Development Managers, Directors, and VPs