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ISRCTN

This system facilitates the registration, reporting, and transparency of clinical research studies, specifically focusing on trials involving medicinal products. It offers key features such as streamlined online submission for study registration, tools for uploading and managing results and summaries, guidance resources to ensure compliance with regulatory standards, and a dedicated platform to promote openness, accountability, and accessibility in clinical research, thus addressing the needs of researchers, sponsors, regulatory bodies, and participants seeking trustworthy and transparent medical studies.

ISRCTN can be found in Clinical Trial Management categories.

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LinkedIn: Visit

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Year Established: 2005

Consumer Type: B2B

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ISRCTN Main Features

Results publishing
Summary of results must be published within 12 months after the study is finished.
Guidance and support
Guidance documents and support are available for registration and results reporting.
Participant summaries
Participants should be offered a clear and easy-to-understand summary of the results.
Results sharing system
A new online system will soon let users upload and share study results easily.
Easy study registration
Registering a study is simple using ISRCTN’s online form, with help available.
Registration of studies
Studies involving medicines must be registered in a public registry.
Supporting transparency
ISRCTN helps researchers and sponsors meet rules for open and transparent research.
UK regulations compliance
New rules apply to UK clinical trials involving medicines, starting from 28 April 2026.

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Home › All Categories › Clinical Trial Management › ISRCTN

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