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The International Recognition Procedure (IRP) for Medicinal Products in the UK

Understanding the Differences Between Medical Devices with Ancillary Substances and Substance-Based Medical Devices

Seamless Transition to eCTD in Ukraine: Discover Our Services

Sharing the power of teamwork!

Revised ICH guideline Q2(R1) on Validation of Analytical Procedures

When to Submit a New 510(k) for Medical Device Changes?

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Valentyna Starodub
Founder and Chief Executive Officer

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