Regulatory Rapporteur October 2020
Focus: Medical technologies Plus: • CPD - Insights on expedited drug development pathways • ATMPs - An overview of advanced therapy regulation in the EU • Strategic planning - How to do regulatory affairs strategic planning well
Regulatory Rapporteur October 2020 (full issue)MEMBERS
Regulatory approval of medical device software and digital health devicesMEMBERS
An overview of advanced therapy regulation – part I: the EUMEMBERS
Regulatory affairs strategic planning: how to do it wellMEMBERS
Devices without a medical purpose: how do they fit into the MDR?MEMBERS
Interview: Lessons for a full lifecycle in pharmaMEMBERS
Current use of artifificial intelligence in the MedTech industriesMEMBERS
Interview: Giving support to the Irish Medtech sector PUBLIC
Editorial: Keeping pace with rapid changes in medical technology PUBLIC