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Clinical Trials Database
๐Ÿ‡ฌ๐Ÿ‡ง United Kingdom

๐Ÿ‡ฌ๐Ÿ‡ง United Kingdom Clinical Trials Database

Search 22,000+ clinical trials conducted in United Kingdom. Access comprehensive trial data including phases, sponsors, outcomes, and locations from ISRCTN & International Registries. Part of Pure Global AI's free database with 840,000+ trials worldwide.

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22,000+ Trials
Search United Kingdom Clinical Trials
Search 22,000+ clinical trials in United Kingdom. Enter disease, drug name, sponsor, or trial ID...
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Frequently Asked Questions
Common questions about the United Kingdom clinical trials database

What is the UK clinical trials database?

The UK clinical trials database contains over 22,000 clinical trials registered through ISRCTN and international registries. The UK is one of the world's leading locations for clinical research.

How do I search for clinical trials in the UK?

Enter a disease name, drug name, sponsor, or trial ID in the search box. Results include trials conducted in the UK from multiple registries.

What regulatory body oversees clinical trials in the UK?

MHRA (Medicines and Healthcare products Regulatory Agency) oversees clinical trials in the UK. The Health Research Authority (HRA) provides ethical approval.

Is this database free to use?

Yes, this database is completely free. Pure Global AI provides free access to help researchers and companies navigate UK clinical research.

What types of trials are common in the UK?

The UK has strong research in oncology, vaccines, genomics, and rare diseases. The NHS provides access to comprehensive patient data and diverse populations.

How has Brexit affected UK clinical trials?

Post-Brexit, the UK has developed its own regulatory framework. The MHRA aims to be a leading global regulator with efficient approval pathways.

About This Database

This database provides free access to clinical trial data from the United Kingdom. The UK has world-class research institutions and the NHS provides unique access to patient populations. Use this tool to find UK trials and understand MHRA requirements.