Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Medical devices are an essential part of the delivery of high-quality healthcare and their procurement and management in the European hospital setting is often under the authority of hospital pharmacists. To support its members, the European Association of Hospital Pharmacists (EAHP) has shared new resources to assist with the handling of medical devices.
To further improve the safety of medical devices for European patients, a new regulatory regime was adopted in spring 2017 encompassing both the Medical Device Regulation (MDR) and the Invitro Medical Device Regulation. With the MDR becoming fully applicable from May 2021 onwards, EAHP has joined forces with EURO-PHARMAT, one of the Association’s members based in France whose work focuses on medical devices. Together with EURO-PHARMAT, a list of medical device resources was created to …
Competing interests None declared.
Provenance and peer review Commissioned; internally peer reviewed.