The 2nd Medical Devices: Regulatory and Compliance Summit is dedicated to classification, conformity assessment and risk management in regulatory strategies to achieve compliance.
Key Topics
Clinical affairs: data, evidence, equivalence and performance studies Achieving a smooth market access
Overview of new guidelines, regulations and registration requirements Notified body feedback on EU MDR implementation
Risk management changes
UDI implementation: challenges and opportunities
Practical insights from medical device manufacturers
Engaging medical device manufacturers with cybersecurity requirements
Classification of medical devices
Updating technical documentation and labelling
Post-marketing adverse event reporting
Who should Attend
Attendees involved or interested in:
Controls & Robotics
Medical Devices
Device Design
In Vitro Diagnostics
Sterilization
Medical Device Design
Regulatory Affairs
Product Quality
Validation
Research & Development
Combination Products
Design Controls
CMC
Medical Device Engineering
Device Development & Manufacturing
Compliance
Quality Assurance/Control
Supply Chain
Risk Management
Past Events
2nd Medical Devices: Regulatory and Compliance Summit - 20-21 Feb 2020, Meliá Vienna, Austria (86779)
Medical Devices: Regulatory and Compliance Summit 2026
Important
Please, check "Medical Devices: Regulatory and Compliance Summit" official website for possible changes, before making any traveling arrangements
