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Cooley LLP
Jessica Koffel
Jessica Koffel
Cooley LLP
EMA Adopts Revised CTIS Transparency Rules
07 Nov 2023 | European Union
EU Study Investigates Different Models For Directly Shipping Drugs To Patients
18 Sep 2023 | Worldwide
European Commission Adopts Directive Extending Time Lead Can Be Used In PVC Sensors Of IVDs
08 Sep 2023 | European Union
European Commission Publishes Guidance On Transition From Clinical Trials Directive To Clinical Trials Regulation
15 Aug 2023 | European Union
European Commission Publishes MDR And IVDR Factsheet For Non-EU/EEA Countries
14 Aug 2023 | European Union
UK Government Provides Limited Extensions To Recognition Of CE Marks For Medical Devices In Great Britain
14 Aug 2023 | UK
GCP Q&A Clarifies Sponsor Role In Trial-Related Tasks, Provides Other Updates
11 Jul 2023 | European Union
Drug & Medical Device Litigation 2023
10 May 2023 | European Union
European Commission Publishes Proposals To Revise Current EU Pharmaceutical Legislative Framework
10 May 2023 | European Union
European Medicines Agency Publishes Q&A On Clinical Trial Data Transparency
09 Feb 2023 | European Union
European Commission Publishes Updated Q&A On Clinical Trials Regulation
17 Jan 2023 | European Union
European Commission Proposes Amending Transitional Provisions In Medical Devices And In Vitro Diagnostics Regulations
13 Jan 2023 | European Union
European Commission Publishes Updated Q&A On The Clinical Trials Regulation
10 Jan 2023 | European Union
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
10 Jan 2023 | European Union
European Commission Proposes Extending Transition Period Foreseen In Medical Devices Regulation
19 Dec 2022 | European Union
New European Manual On Borderline Classification For Medical Devices And IVDs
09 Dec 2022 | European Union
Productwise Bitesize: In Vitro Diagnostic Medical Devices Regulation
19 Aug 2022 | United States
Medical Devices Regulation
14 Jul 2022 | European Union
Draft Common Specifications For Products Without An Intended Medical Purpose
02 Mar 2022 | European Union
Productwise Bitesize: Clinical Trials Regulation
26 Jan 2022 | European Union
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