MDRG 27/07/2023 MDRG 27/07/2023 EUDAMED Notified Bodies & Certificates Module Update 🔥 Read More MDRG 26/07/2023 MDRG 26/07/2023 Updated Actor Module for EUDAMED ✅ Read More MDRG 25/07/2023 MDRG 25/07/2023 MHRA Timeline on Implementation of Regulations ⏳ Read More MDRG 24/07/2023 MDRG 24/07/2023 MDCG 2022-18 ADD.1 - Application of Article 97 MDR to legacy devices ⚡ Read More MDRG 21/07/2023 MDRG 21/07/2023 FDA Guidance on Content of Premarket Submissions for Device Software Functions 📢 Read More MDRG 20/07/2023 MDRG 20/07/2023 Updated EU Harmonised Standards for Sterilization IVDR (EU) 2023/1411 📰 Read More MDRG 19/07/2023 MDRG 19/07/2023 Updated EU Harmonised Standards for Sterilization MDR (EU) 2023/1410 🔍 Read More MDRG 18/07/2023 MDRG 18/07/2023 New MDR Notified Body – HTCert 🆕 Read More MDRG 17/07/2023 MDRG 17/07/2023 Cosmetics Regulation Updates Hazardous Substances List 💥 Read More MDRG 14/07/2023 MDRG 14/07/2023 Team-NB Organizes Training Session on IVDR Technical Documentation for Manufacturers 📚 Read More MDRG 13/07/2023 MDRG 13/07/2023 Master Unique Device Identification (UDI-DI) for Highly Individualized Devices in the EU 👍 Read More MDRG 16/06/2023 MDRG 16/06/2023 EU Released Summary of Coverage of Codes by Notified Bodies Read More MDRG 15/06/2023 MDRG 15/06/2023 MDCG 2023-3 Q&A on vigilance terms and concepts as outlined in the MDR Read More MDRG 14/06/2023 MDRG 14/06/2023 Enhancing Consistency and Quality: IMDRF Releases Guidance on Medical Device Regulatory Review Reports Read More MDRG 13/06/2023 MDRG 13/06/2023 Published Overview of Ongoing guidance development and deliverables of MDCG Subgroups Read More MDRG 12/06/2023 MDRG 12/06/2023 New MDR NB – SZUTEST Konformitätsbewertungsstelle GmbH Read More MDRG 09/06/2023 MDRG 09/06/2023 EU Q&A on MDR Transitional Period Proposal Read More MDRG 08/06/2023 MDRG 08/06/2023 FDA Cybersecurity Guidance Released Read More MDRG 07/06/2023 MDRG 07/06/2023 Regulatory Intelligence Newsletter Read More MDRG 06/06/2023 MDRG 06/06/2023 MDR Amendment 2023/607 published and effective as of 2023-03-20 Read More Newer Posts Older Posts
MDRG 24/07/2023 MDRG 24/07/2023 MDCG 2022-18 ADD.1 - Application of Article 97 MDR to legacy devices ⚡ Read More
MDRG 21/07/2023 MDRG 21/07/2023 FDA Guidance on Content of Premarket Submissions for Device Software Functions 📢 Read More
MDRG 20/07/2023 MDRG 20/07/2023 Updated EU Harmonised Standards for Sterilization IVDR (EU) 2023/1411 📰 Read More
MDRG 19/07/2023 MDRG 19/07/2023 Updated EU Harmonised Standards for Sterilization MDR (EU) 2023/1410 🔍 Read More
MDRG 14/07/2023 MDRG 14/07/2023 Team-NB Organizes Training Session on IVDR Technical Documentation for Manufacturers 📚 Read More
MDRG 13/07/2023 MDRG 13/07/2023 Master Unique Device Identification (UDI-DI) for Highly Individualized Devices in the EU 👍 Read More
MDRG 16/06/2023 MDRG 16/06/2023 EU Released Summary of Coverage of Codes by Notified Bodies Read More
MDRG 15/06/2023 MDRG 15/06/2023 MDCG 2023-3 Q&A on vigilance terms and concepts as outlined in the MDR Read More
MDRG 14/06/2023 MDRG 14/06/2023 Enhancing Consistency and Quality: IMDRF Releases Guidance on Medical Device Regulatory Review Reports Read More
MDRG 13/06/2023 MDRG 13/06/2023 Published Overview of Ongoing guidance development and deliverables of MDCG Subgroups Read More
MDRG 06/06/2023 MDRG 06/06/2023 MDR Amendment 2023/607 published and effective as of 2023-03-20 Read More
