anteris and Bellingswood regularly organize network meetings and workshops on various topics related to the regulatory requirements of medical devices. The aim of these events is to promote a platform for the exchange of experience among specialist colleagues and to inform about the latest developments in the area of regulatory affairs.

Our first event covering MDR/IVDR and Clinical Evaluation in Munich, last October, was completely sold out. Experts from the biotech, pharmaceutical, and medical device industries, such as developers and manufacturers, CROs, market researchers, and consultants, discussed the latest developments and challenges of new regulations concerning medical devices, drug/device combination products, and IVD devices.

Agenda overview:

MDR / IVDR and combination products / companion diagnostics

  • Clinical evaluation of medical devices under MEDDEV 2.7.1 Rev.4. What are the first experiences and expectations by the notified bodies?
  • Combination Products - integrating medical devices in the pharma world - challenges and lessons learned
  • Requirements of the IVDR for companion diagnostics
  • Requirements of post market surveillance with medical devices under the MDR
  • Guided tour through the "Pharmazie-Historisches Museum"
  • Networking and apéro


Date: Friday 9th of March 2018, 1:30 - 5:30 PM, Pharmacy Museum Basel
Contribution to expenses: 85 CHF

For further informations please contact Carola Seitz. She will be happy to answer any questions concerning agenda or organizational queries.

Thank you for being interested in our network event. We are sorry, registrations are not possible anymore.



Agenda overview

PDF download

anteris medical GmbH supports the pharmaceutical, biotech and medical device industries globally by managing the development of combination products, medical device products or in vitro diagnostics. With our comprehensive service, we offer an efficient approach to the development and technical documentation of your planned product, as well as innovative solutions to regulatory issues and tailor-made marketing and sales strategies.

Bellingswood MedTech is a consulting company for regulatory requirements of medical devices and drug combination products. With our multidisciplinary teams of highly qualified experts, we provide a wide range of regulatory and clinical expertise such as global registrations, clinical evaluations and biocompatibility assessments.



Next Experience Network Events

Topic: MDR/IVD and Drug Combination Products 

Date: Basel, March 9th 2018