„Consequences of the Medical Devices Regulation (MDR) for Notified Bodies and Manufacturers” Interview with our Managing Director, Klaus-Dieter Ziel for the MPJ- Journal for Medical Devices

In the latest issue of the German Journal for Medical Devices, MPJ-Medizinprodukte-Journal, you find an interview with the Managing Director of MEDCERT GmbH. On several pages the topics such as: preparation of a Notified Body for the MDR, questions regarding re-certification under the MDD, transition periods, impacts of Brexit and differences between MDD and MDR, are addressed in more detail.

You get the interview here.

• „Consequences of the Medical Devices Regulation (MDR) for Notified Bodies and Manufacturers” Interview with our Managing Director, Klaus-Dieter Ziel for the MPJ- Journal for Medical Devices
• MEDCERT: Merry Christmas!
• EU: Designation Process for Notified Bodies under the MDR
• EU: EU Commission updates its lists of harmonized standards
• MEDCERT: Application for the Designation as Notified Body under the MDR – Medical Device Regulation