Newsletter December 2017
- EU: DELTA-Checklist ISO 13485:2016
- „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