Medical Devices: The role played by regulations in terms of developing and transforming a prototype into a certified product

Date01-12-2021 - 01-12-2021 Date

Online | 15:00 - 15:30 h | 30 minutes

Tekniker Sharing Events, webinar, medical devices, regulations, ISO13485, IEC62304, IEC60601

Jon Mabe
Director of Electronics and Communications

This webinar will explain the challenge of matching regulatory requirements applied to medical devices, that feature electronic hardware and software (ISO13485, IEC62304, IEC60601), to agile and iterative processes required to develop and transform prototypes into certified and marketable products.

Register here

All registration data you are about to supply are the responsibility of Tekniker; data shall be managed via the GoToWebinar application supplied by Logmein (California, USA) that will be used for this sole purpose pursuant to a data protection agreement that ensures compliance with European data protection regulations (RGPD).

For more information

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.