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  • Updates

Get ready for serious incident reporting under the AI Act
  • Updates

Starodub & Greijmans Regulatory Consultancy B.V. announce a new strategic regulatory partnership
  • Updates

Distribution of Medical Device Software via app stores
  • Updates

“Medical” in medical devices: the often-forgotten element
  • Updates

Don’t let GSPR be the weakest link in your MDR submission
  • Updates

Quality, Operations & Improvement services
  • Updates

EU eCTD Update – Implementation of Module 1 v3.1.1 & Validation Criteria v8.2
  • Updates

EU-Japan Biotech Mission & BioJapan 2025
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Selection of non-clinical models for ATMP development
  • Updates

BioEurope Vienna 3 – 5 November 2025
  • Updates

Have you explored our white paper on the nIVD MA ToC yet?
  • Updates

Understanding new post-market surveillance requirements for medical devices
  • Updates

Palleos and Starodub Announce Strategic Partnership to Streamline Regulatory Pathways for Clinical Trials
  • Updates

Starodub B.V. is heading to China!
  • Updates

Festival of Biologics 30 September – 2 October 2025, Basel
  • Updates

Beyond Pride Month: Building Inclusion Every Day
  • Updates

GMP Guidelines: Rapid advancement of digital technologies and the implementation of AI
  • Updates

First Joint Clinical Assessments (JCAs) begin under EU HTA Regulation
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Gilliian Marland
Senior RA Consultant
Gilliian Marland

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