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Re­sour­ces & Trai­ning

Dive into our ex­ten­si­ve know­ledge hub, fea­turing blogs, events, white­pa­pers, and more. Stay informed and ahead of the curve with expert insights and re­sour­ces designed to support your journey in ma­nage­ment systems and cer­ti­fi­ca­ti­ons.
Schulung

Re­gis­tra­ti­on of Medical Devices in China – Fun­da­men­tals and Key Re­qui­re­ments

Feb. 03 , 2027, 09:00-13:00
Online | English
Schulung

Supplier Ma­nage­ment and Com­pli­ance under ISO 13485

Juli 23 , 2027, 09:00-12:00
Online | English
Schulung

Ve­ri­fi­ca­ti­on vs. Va­li­da­ti­on Medical Devices

Apr. 09 , 2027, 09:00-12:00
Online | English
Schulung

Risk ma­nage­ment ac­cor­ding to MDR & ISO 14971 (Ad­van­ced)

März 04 , 2027, 09:00-15:00
Online | English
Schulung

Risk ma­nage­ment ac­cor­ding to MDR & ISO 14971 (Basic)

März 03 , 2027, 09:00-15:00
Online | English
Schulung

MDR Basics

Aug. 31 , 2027, 09:00-13:00
Online | English
Schulung

ISO 13485 Quality Ma­nage­ment System In­tro­duc­tion

Juni 16 , 2027, 09:00-12:00
Online | English
Schulung

Tech­ni­cal Do­cu­men­ta­ti­on under MDR

Mai 20 , 2027, 09:00-15:00
Online | English
Schulung

GSPR Es­sen­ti­als: Com­ply­ing with Annex I of the EU Medical Device Re­gu­la­ti­on

Jan. 21 , 2027, 09:00-13:00 - Aug. 10 , 2027, 09:00-13:00
Online | English