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FDA eMDR – Electronic Medical Device Reporting

Update: April 10, 2026

The FDA has updated its Electronic Medical Device Reporting (eMDR) framework, confirming the transition to the ESG NextGen Unified Submission Portal

As of April 14, 2025, the ESG NextGen portal replaces the legacy WebTrader interface, providing a web-based platform to submit regulatory information and track submission status

 

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Recentes

  • EMA Article 57 Q&A Version 1.15 (9 September 2026)
  • EMA guidance on Electronic product information (ePI) submission during centralised procedures
  • EU Medical Device Regulation (2017/745) and In Vitro Diagnostic Medical Device Regulation (2017/746) – Impact on international registrations. Middle East and Africa focus
  • IMDRF Document Implementation Report. 1 September 2026
  • EU Regulatory News : IVD Classification Rules – MDCG 2020-16 Rev.5
  • Revised version of EU GMP Annex 19: Reference and Retention Samples
  • Evaluation of Therapeutic Equivalence. Guidance for Industry
  • FDA Considerations for the Regulation of Generative Al-Enabled Medical Devices: Discussion Paper and Request for Feedback

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