The Medical Device Safety and Reporting Summit 2019 covers topics such as:
- 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
The Medical Device Safety and Reporting Summit 2019 brings together 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
