EMA - Medical devices: new guidance for industry and notified bodies
Year: 2024
Type: other
Abstract: A new revision of the guidance available to applicants, marketing authorisation holders and notified bodies of medical devices has been published today. This question-and-answer document provides practical considerations on the implementation of the medical devices and in vitro diagnostic regulations for combinations of medicinal products and medical devices. More information on the EMA Website.
Source: OpenEdition (OpenEdition)
DOI: 10.58079/12f8x
Author: Vroby
Language: English
Topic: Healthcare Regulation
Subfield: Health Information Management
Field: Health Professions
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W6899292092
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