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 06 Feb 2023 EMA To Reinstate Its Proactive Clinical Data Publication Policy United States Consumer
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