Panel Discussion: Preparing for MHRA’s Most Significant Update in Two Decades
Live Panel Discussion | 26 March 2026 | 3:00pm GMT / 10am EST
From 28 April 2026, the Medicines and Healthcare products Regulatory Agency (MHRA) will make major changes to how clinical trial records are kept. Sponsors will need to make sure the Trial Master File (TMF) and other key trial documents are complete, secure, and easy to access over the long term.
The 2026 update also follows ICH E6(R3) and highlights the need for better long-term record management.
In this session, we will cover:
- How the new rules affect clinical trial records
- Key compliance and practical issues for sponsors
- What organisations should do now to get ready
Expert panel
- Sandra Blake, Corporate Records Manager, Barts Health NHS Trust
- Sarah Hitching, Hedian Records Management
- Matthew Addis, Founder & CTO, Arkivum
Who should attend?
Pharma sponsors, CROs, regulatory and QA leaders, clinical operations teams, IT, Record Managers and compliance professionals who need clear guidance on the MHRA changes.
Anthony Wells
Anthony assumed the role of Product Marketing Manager at Arkivum in 2024, leveraging over a decade of experience of product marketing management in the technology sector. Proficient in developing and executing marketing strategies, Anthony is also experienced in product lifecycle management, from inception through to discontinuation.
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