R Clinic on Understanding documentation […]
Mentor Mixer on Understanding of EU MDR 2017/745 for European Approval
Mentor Mixer on Understanding of […]
R Clinic on Understanding documentation requirements under EU MDR 2017/745
R Clinic on Understanding documentation […]
R Clinic on Planning Regulatory Pathway & Essential Requirements for Medical Devices & IVDs
R Clinic on Planning Regulatory […]
VBC on ISO 13485:2016 Medical Devices QMS & Internal Auditor Training Course
Venture Base Camp on ISO […]
VBC on Requirements of the Medical Device Regulation (MDR) for CE marking
Venture Base Camp on Requirements […]
VBC on ISO 13485:2016 Medical Devices QMS & Internal Auditor Training Course
Venture Base Camp on ISO […]
R Clinic on Essential Regulatory Requirements for Medical Devices in EU, MDSAP & ISO 13485
When? – Friday, 29 April […]