Preparing for the Upcoming EU Medical Device Regulations 2016 is a webinar that covers topics such as:
- Timeline for transition to the new regulations
- Scope of the new regulations
- New requirements for manufacturers, distributors, reprocessors and independent bodies
- Emphasis on high-risk devices with greater transparency and traceability
- Q&A
- Additional clinical trial requirements
Preparing for the Upcoming EU Medical Device Regulations 2016 is intended for attendees from device distributors, manufacturers and testers responsible for:
- Quality Testing
- Production
- Distribution
- Quality Assurance
- Clinical Testing
- Packaging and Labeling
- Post-Marketing Surveillance
- Product Recall and Withdrawal
- Regulatory Staff
- Consumer/Patient Complaints and Adverse Event Reporting
- Audit Staff
