Article 18 Sep 2023 EU Study Investigates Different Models For Directly Shipping Drugs To Patients Worldwide Healthcare
Article 08 Sep 2023 European Commission Adopts Directive Extending Time Lead Can Be Used In PVC Sensors Of IVDs European Union Healthcare
Article 15 Aug 2023 European Commission Publishes Guidance On Transition From Clinical Trials Directive To Clinical Trials Regulation European Union Healthcare
Article 14 Aug 2023 European Commission Publishes MDR And IVDR Factsheet For Non-EU/EEA Countries European Union Healthcare
Article 14 Aug 2023 UK Government Provides Limited Extensions To Recognition Of CE Marks For Medical Devices In Great Britain United Kingdom Healthcare
Article 11 Jul 2023 GCP Q&A Clarifies Sponsor Role In Trial-Related Tasks, Provides Other Updates European Union Healthcare
Article 10 May 2023 European Commission Publishes Proposals To Revise Current EU Pharmaceutical Legislative Framework European Union Privacy
Article 14 Mar 2023 The Council Of The European Union Votes In Favor Of Amending The Transitional Provisions In The MDR And IVDR European Union Healthcare
Article 13 Mar 2023 EMA Launches Pilot Program For Expert Panel Scientific Advice In Relation To Certain High-risk Devices Belgium Healthcare
Article 23 Feb 2023 The European Parliament Votes In Favor Of Amending The Transitional Provisions In The MDR And The IVDR European Union Consumer
Article 09 Feb 2023 European Medicines Agency Publishes Q&A On Clinical Trial Data Transparency European Union Healthcare
Article 06 Feb 2023 EMA To Reinstate Its Proactive Clinical Data Publication Policy United States Consumer
Article 31 Jan 2023 New Applications For Approval Of Clinical Trials To Be Submitted In Accordance With The CTR Starting On 31 January 2023 European Union Consumer
Article 17 Jan 2023 European Commission Publishes Updated Q&A On Clinical Trials Regulation European Union Healthcare
Article 17 Jan 2023 The EMA Publishes Updated Q&A On Clinical Trial Sponsor Oversight Of Delegated Tasks United States Compliance
Article 16 Jan 2023 EMA Guideline On Sponsor Responsibility For Release And Shipping Of IMPs In Accordance With GCP And GMP In The EU Comes Into Effect European Union Compliance
Article 13 Jan 2023 European Commission Proposes Amending Transitional Provisions In Medical Devices And In Vitro Diagnostics Regulations European Union Healthcare
Article 10 Jan 2023 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 European Union Consumer