The role of GLP in Medical Device biocompatibility testing Göran Stjernström2022-11-03T14:19:13+00:00October 11th, 2021|
How to save time and money with a literature review of clinical data Göran Stjernström2022-11-03T14:23:56+00:00October 8th, 2021|
Medical Device software life cycle processes – IEC 62304 – an overview Göran Stjernström2022-11-03T14:30:59+00:00October 8th, 2021|
Post Market Clinical Follow-Up for a Medical Device – How to reach MDR Requirements? Göran Stjernström2022-11-03T14:28:44+00:00October 8th, 2021|
