Parapharmazien in Frankreich Archives

Apotheken versus Parapharmazien in Frankreich

by Maria Klaas | Apr 22, 2020 | Deutsche Beiträge

April 2020, Maria Klaas – Apotheken versus Parapharmazien in Frankreich. Drastische Veränderungen im Apotheken-Sektor in Frankreich. Viele Medzinprodukte werden im Unterschied zu Deutschland in Frankreich von Apotheken bzw. Parapharmazien verkauft.

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Latest Insights

GTAI has created a special page on sanctions and the consequences of the war in Ukraine.
Internet platform for medical needs in Ukraine by the German initiative Medical Bridge.eu
Swissmedic refers to a leaflet on the obligations for authorised representatives, importers and distributors
European industry association for digital assistive technology DATEurope founded in early 2021. DAT includes aids for communication, for the blind and visually impaired, for environmental control, assistive call systems, software tools and robotics.
New web portal for the list of medical aids according to §139 SGB V of the GKV-Spitzenverband: for reference and online application
Revised guidance on "Designation of a Swiss authorised representative under the new MepV" of 29 January 2021, addressed to Swiss distributors and importers.
Overview of all assessments of new examination and treatment methods (NUB) by the G-BA
28 Notified Bodies are now accredited. Currently (April 2022) there are 7 in Italy, 2 in Finland, 3 in the Netherlands and 7 in Germany; in addition, one each in Belgium, Slovakia, Hungary, Norway, France, Sweden, Slovenia, Ireland and Croatia. Nando database
the MHRA in the UK has published a guidance document for manufacturers and distributors of medical devices
BfArM included the first “apps on prescription” in the new directory for digital health applications (DiGA) in early October 2020
new standalone UKCA mark after Brexit; current EU CE marking will still be in operation for Medical Devices and invitro diagnostic in Great Britain until June 2023
EU-implementation regulation for the reprocessing of disposable products, valid from 26 May 2021
FDA increases medical device registration fees from October 2020
The European Commission published the new “Clinical evaluation assessment report template” of the Medical Devices Coordination Group (MDCG) on 17 July 2020
On 1 July 20, the Swiss Federal Council adopted the revision of the Regulation on Medical Devices (MepV) and the new Regulation on Clinical Trials for Medical Devices (KlinV-Mep). As a result, Switzerland remains subject to EU medical device law.
In-vitro-diagsnostics must be re-evaluated according to the new IVDR by 26 May 2022.
The new In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 has entered into force. It must be implemented for products... with higher risk by May 2025, ...with lower risk class C by May 2016, ...with lower risk classes B and A by May 2027
The European Council postpones the application of EUDAMED by two years until May 2022