Facilitating European Clinical Research

ECRIN, the European Clinical Research Infrastructure Network,  facilitates multinational clinical research, through the provision of advice and services for the set-up and management of investigator or SME led clinical studies in Europe. ECRIN unites national networks of clinical trial units across Europe, through its scientific partners, to fulfil its vision of generating scientific evidence to optimise medical practice.

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13 Members & Observer Countries
130 CTUs in our network
361 Million citizens represented
75 Trials in ECRIN portfolio

ECRIN Tools

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Adaptive Platform Trials Toolbox

Adaptive Platform Trial Toolbox

The Adaptive Platform Trial Toolbox aims to collect the accumulated knowledge, experience, and resources (collectively termed as ‘tools’) from multiple projects and trials into a practical and guided toolbox to facilitate planning and conduct of future adaptive platform trials in any therapeutic area. 

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CRMDR Clinical Research Metadata Repository

Clinical Research Metadata Repository

The Clinical Research Metadata Repository is the free online tool to help scientific researchers find documents and data linked to a clinical research study, and to obtain information on the accessibility of those results.

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Rare disease clinical trial toolbox

Rare Diseases Clinical Trials Toolbox

The toolbox aims to collect the accumulated knowledge, experience, and resources generated by previous projects and/or research infrastructures and other organisations into a practical and guided toolbox to help understand the regulations and requirements for conducting trials, with special focus on investigator-initiated trials for rare diseases. 

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Paediatric clinical research toolbox

Paediatric Tools

A series of tools and procedures to support the setup and management of multinational neonatal and paediatric clinical trials in Europe were developed through the PedCRIN project.

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Risk Based Monitoring Toolbox

Risk Based Monitoring Toolbox

The Risk-Based Monitoring Toolbox provides information on tools available for risk assessment, monitoring and study conduct, the institutions where they are used, and other relevant details such as links and user feedback.

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ECRIN Regulatory Ethical clinical trials

Regulatory and Ethical Tools (RED)

ECRIN RED is a central resource for information about clinical trial regulatory and ethical requirements covering a number of European countries and multiple study types such as clinical drug trials, clinical investigations of medical devices, combination drug-device studies and nutritional studies.