meddevo
HomeAboutResourcesContact
Demo
Posted on 
August 14, 2020

EU-MDR GSPR Management

The central point of compliance under MDR is ANNEX 1: General Safety and Performance Requirements (GSPR).

At first sight, the document looks exactly like you know it for ANNEX 1 under MDD. But the requirements are now stricter. At the same time, the requirements to make the technical documentation clearer and more unambiguous have also increased. In this Video we talk about the GSPR Management.

Tagged:
GSPR
ANNEX I
MDR
State of the art
Michael M. Kania
CEO, FOUNDER
view All Posts
Featured Posts
Medical Device Regulation
Integrated e-IFU Solution
Medical Device Regulation
From OEM to Contract Manufacturer
Medical Device Regulation
TÜV Rheinland: EU-MDR & Digitalization
Medical Device Regulation
State of the art GSPR
Tags
ANNEX I
Article 22
Development
GSPR
MDR
Meddevo
OEM
Setpacker
State of the art
eIFU
Subscribe
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
Stay Connected

Try meddevo

Demo
More Posts

You Might Also Like

Medical Device Regulation
Integrated e-IFU Solution
Oct 26, 2020
 by 
Simon Schenk
Medical Device Regulation
From OEM to Contract Manufacturer
Sep 26, 2020
 by 
Michael M. Kania
Medical Device Regulation
TÜV Rheinland: EU-MDR & Digitalization
Aug 31, 2020
 by 
Johann Töws
Medical Device Regulation
State of the art GSPR
Aug 10, 2020
 by 
Michael M. Kania
Medical Device Regulation
Systems and Procedure Packs under MDR
Aug 1, 2019
 by 
Michael M. Kania
meddevo

eTD and eQMS solution for medical devices
Made in Germany

Navigation
HomeAboutContact
Other Links
TeamImpressumDatenschutzerklärung
Copyright ©2020 by meddevo. All rights reserved.