Peter Fry

Country Manager UK at QbD Group

Peter leads QbD Group's UK operations as Country Manager, driving business growth and delivering life science consulting services across the United Kingdom.

5 articles

Regulatory AffairsSep 30, 2025 2 min

EU New Variations Guidelines to Streamline Lifecycle Management of Medicines

The European Commission has published the final version of the new Variations Guidelines for human medicines, which will take effect on 15 January 2026 and are designed to support the new Variations Regulation that entered into force in January 2025.

Regulatory AffairsMay 7, 2025 5 min

eCTD Publishing: 10 Tips for a Smooth Submission Process

Learn how to streamline your eCTD publishing and submissions with 10 expert tips. Avoid pitfalls, ensure compliance, and meet global regulatory requirements.

Regulatory AffairsSep 4, 2024 6 min

Mastering EU Product Information: The Role of the EMA’s Linguistic Review Process in Centralised Procedures

Explore essential insights into the EMA Linguistic Review process for Product Information of medicinal products approved via the Centralised Procedure.

Regulatory AffairsMar 21, 2024 3 min

MHRA to Launch RegulatoryConnect Portal in the UK: A New Era in Regulatory Management

Learn how the MHRA's RegulatoryConnect Portal simplifies UK regulatory management, offering improved efficiency and innovation in healthcare regulation.

Regulatory AffairsMar 14, 2023 2 min

UK's medicines regulator announces IT roadmap

The UK's MHRA is developing a new IT system to streamline submissions related to product licensing and process licensing. Read more here.

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