TypeAllBlog & InsightsCase studiesEvents & ConferencesIVD NewsRegulatory UpdatesWhitepapers
SectorAllDigital Health & AIIVDsLaboratoriesMedical DevicesPrecision Medicine & CDx
Clinical Investigation Report for Medical Devices (2023/C 163/06): Preparing your CIR template

Clinical Investigation Report for Medical Devices (2023/C 163/06): Preparing your CIR template
10.05.2023
Blog & Insights | Medical Devices
Impact of Spain’s Real Decreto 192/2023 on Clinical Investigations with Medical Devices

Impact of Spain’s Real Decreto 192/2023 on Clinical Investigations with Medical Devices
22.04.2023
Regulatory Updates | Medical Devices
EU Q&A Guide: Amendments to MDR and IVDR Transitional Provisions

EU Q&A Guide: Amendments to MDR and IVDR Transitional Provisions
27.03.2023
Regulatory Updates | IVDs, Medical Devices
Clinical Investigation Submission Spain AEMPS: What You Need to Know About the Updated Process

Clinical Investigation Submission Spain AEMPS: What You Need to Know About the Updated Process
13.02.2023
Blog & Insights | Medical Devices
Understanding MDCG 2020-10 Rev 1: Safety Reporting in Medical Device

Understanding MDCG 2020-10 Rev 1: Safety Reporting in Medical Device
21.11.2022
Blog & Insights | Medical Devices
Clinical Evaluation Consultation Procedure (CECP) – New Opinion Issued

Clinical Evaluation Consultation Procedure (CECP) – New Opinion Issued
24.10.2022
Blog & Insights | Medical Devices
Request the Precision Medicine Services Pack​
Gain access to MDx’s Precision Medicine Services Pack—detailing our capabilities in clinical research, regulatory strategy, and companion diagnostics. Learn how we support pharma, CDx, and advanced therapy developers across the clinical and regulatory lifecycle.
We respect your privacy. All information submitted will 
remain confidential.
Checkboxes