Master The Legal Implications Of The EU MDR With Expert Advice, Case Studies And Interactive Discussions
Get To Grips With Legislation And Legal Challenges For Medical Device Manufacturers
With Leading Lawyers, Competent Authority And Notified Body Perspectives
2020 Highlights: Navigate The Legal Challenges Of The EU MDR
前监管Challen专家法律建议ges
前监管Challen专家法律建议ges
- Transitional provisions under the EU MDR: What constitutes a "significant change"?
- Can you legally challenge decisions of your Notified Body? Find out the current state of play...
- Claims requirements: Talking labelling, advertising & instruction
Practical Legal Challenges: Solutions And Advice
Practical Legal Challenges: Solutions And Advice
- Roles, responsibility and liability for the Person for Responsible for Regulator Compliance (PRRC)
- EU MDR & new Product Liability Directive: Hear the latest on liability claims
- Delve into IP & data compliance for digital data and AI
Elsewhere At The MedTech Summit...
Elsewhere At The MedTech Summit...
- Attend ourEU Medical Device Regulationtrack for comprehensive coverage of the latest regulatory guidance, case studies and lessons learned under the EU MDR
- Join ourEU IVD Regulation and Strategytrack to get updates and hear first-hand experiences of EU IVDR implementation
- Hear the latest regulatory developments from around the world in ourMedical Device Regulatory Affairs in Global Marketstrack