Medical Device Safety and Reporting Summit 2019

Topics

• Best practices and guidelines for medical device monitoring and safety with a post-approval surveillance strategy
• Ensure medical devices meet proper regulatory requirements and the highest quality standards
• Allow patients to access high-quality devices with innovative strategies to maintain compliance with the FDA
• Recognize future regulation implications and ensure a successful risk management plan
• Essential elements of an effective corrective and preventive action (CAPA) system

Who should Attend

Attendees from:

• Clinical Quality Management
• Quality Management
• Regulatory Affairs
• Quality Assurance
• Medical Device
• Medical Affairs
• Compliance/Ethics
• Risk Assessment
• Site Management
• Monitoring
• Research and Development
• Site Quality
• Pharmacovigilance
• Project Management
• Data Management
• Safety
• Adverse Events/Case Management Service Providers
• Real-World Evidence
• Healthcare/Pharmacovigilance Consultants
• Safety Database Providers
• CROs
• Technology Vendors