6
Dec 2019 10:30 - 16:00

Privileged Talks - The EU Medical Devices Regulation. Is the medtech ecosystem ready?

Format Face to face
Language ENGLISH
Location Lecture Hall 01 - via Bocconi 8 - Milano

Privileged TalksĀ are exclusive conversations with Top European policy makers.

Ā 

A unique opportunity to take part in ourĀ exclusive debate on the new EU Medical Devices Regulation coming into force on 26 May 2020 with European Commission and FDA's Representatives:

Ā 

  • Salvatore Dā€™Acunto, Head of the Health and Cosmetics Unit, DG GROW, EC
  • Salvatore Scalzo, Policy and Legal Officer at DG GROW, EC
  • Ritu Nalubola, Director, of FDA Europe Office

Ā 

Bringing together the international protagonists of the heath system, the talks were created to become an exclusive chance for meeting and debating with the policy makers of the European healthcare system.

Ā 

  • How will these new regulations affect competitiveness of the medtech industry?
  • What type, quantity and quality of evidence need to be generated by medtech manufacturers?
  • How will healthcare providersā€™ and patientsā€™ access to innovations be affected?

Ā 

Answers to these and other questions will emerge from the discussion with the EC, FDA, MedTech Europe and European Patients Forum.

Ā 

The participation fee is ā‚¬ 500 (+VAT, if applicable).Ā 

Ā 

For Academics, Public Employees, Members of Patient Associations participation is free, subject to registration.

REGISTER HERE

Ā 

Please feel free to write to silvia.malandrino@sdabocconi.itĀ for any additional information you might need.

Ā 

AGENDA

Related Articles

The global mental health challenge: trends, disparitie...
Authors
Required time 6 min
Public-private hybrids in the Italian healthcare system: ...
Required time 6 min
Biogen: managing healthcare challenges between complexit...
Authors
Required time 6 min