Tag: EU Legislation
The European Parliament votes in favor of amending the transitional provisions in the MDR and the IVDR
The European Parliament approves the European Commission’s proposal to extend the transitional periods in the MDR and remove the “sell-off” deadline in the MDR and IVDR.
Nothing lasts forever: Proposed ban of PFAS in the EU
Emma Bichet and Selma Abdel-Qader
The proposed EU restriction of per-and polyfluoroalkyl substances was published on 7 February 2023. If adopted into law, the restriction will result in a ban on the manufacture, use and placing on the EU market of around 10,000 PFAS,
REACH for the stars!
Emma Bichet, Carol Holley and Selma Abdel-Qader
Cooley’s Productwise Bitesize brings you a short introduction to the REACH Regulation.
Productwise Bitesize: The Cosmetic Products Regulation
Emma Bichet, Harriet Jones and Selma Abdel-Qader
Cooley’s Productwise Bitesize brings you a short introduction to the Cosmetic Products Regulation.
The clock is ticking – feedback period for new EU cyber rules ends soon
Claire Temple, Emma Bichet and Selma Abdel-Qader
Productwise guides you through the European Commission’s new initiative on cybersecurity requirements.
The European Commission publishes a proposal to amend the transitional provisions foreseen in the Medical Devices Regulation and the In Vitro Diagnostic Medical Device Regulation
Elizabeth Anne Wright and Jessica Lauren Koffel
Read an overview of the proposed amendments to the transitional provisions of the MDR and the IVDR.
Medical devices and IVDs fall outside the scope of the proposed CRA – but for how long?
Elizabeth Anne Wright and Alexander Wenzel
The medical device industry is out of scope of the proposed Cyber Resilience Act
The NIS 2 Directive establishes new cybersecurity requirements for medical device manufacturers
Elizabeth Anne Wright and Alexander Wenzel
Cybersecurity requirements established in the NIS 2 Directive apply to medical device manufacturers
European Commission proposes extension of the transition periods foreseen in the Medical Device Regulation
Read our update on the extension of the transition periods in the Medical Device Regulation