Medical Device Regulations & Compliance Summit 2022

Topics

• Improving submissions under eu mdr and ivdr
• Complexities of eu mdr implementation

Who should Attend

Senior attendees with responsibilities in:

• Medical Devices/In Vitro Diagnostics/ Combination Products
• MDR/ IVDR
• Device Development/ Device Engineering
• Regulatory Affairs/ CMC/ Compliance
• Risk Management/ Safety Risk
• Design Controls/Device Design
• Research & Development
• Traceability/ Sterilization
• Post Market Surveillance/ Vigilance
• QA/ QC