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Updates
How ready are you for MDR submission?
January 28, 2025
Updates
Regulatory Affairs: A Marathon of Dedication and Strategy
January 10, 2025
Updates
Looking Back on Milestones and Forward to the Future
December 18, 2024
Updates
Interpretation of Well-Established Technology (WET) under the EU MDR
December 11, 2024
Updates
Medical Devices with Coatings: Impact on Classification
December 5, 2024
Updates
From Formatting to Submission: End-to-End eCTD Support
November 29, 2024
Updates
AI in Medical Devices: Key Highlights of the New Team NB Position Paper
November 25, 2024
Updates
Public consultations on package insert and labelling policy
November 15, 2024
Updates
Starodub is attending Medica 2024
November 7, 2024
Updates
Exciting News from Starodub!
November 6, 2024
Updates
International Side Effects Week: How you can (sometimes) prevent side effects yourself
November 5, 2024
Updates
Comprehensive MDR Compliance: Key Recommendations for Medical Device Manufacturers
November 4, 2024
Updates
Is Your Post-Market Surveillance (PMS) System Fully MDR-Compliant?
October 31, 2024
Updates
Regulatory Affairs, Drug Development & AI: Navigating the New EMA Guidance
October 30, 2024
Updates
Change in distribution Direct Healthcare Professional Communication in the Netherlands
October 23, 2024
Updates
Key Outcomes of LSH Dutch Mission to Japan: New Partnerships to Support Market Entry
October 16, 2024
Updates
Article 61(10) of MDR: A Pathway for Medical Device Software?
October 15, 2024
Updates
The Compliance Compass: Guiding Clinical Investigations for Medical Devices through ISO 14155 and MDR
October 11, 2024
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Iryna Berchak
RA Consultant
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