News

The canSERV project is pleased to introduce the MaP Toolbox, a free, open-access tool designed to support researchers in planning and conducting master protocol clinical trials, including platform, umbrella, and basket trials....

WHO has launched the Global Clinical Trials Forum (GCTF), a global, multi-stakeholder network to strengthen clinical trial environments and infrastructure at national, regional and global levels....

In 'Mapping of Available Infrastructure Services for Large Medical Cohorts', which draws on a survey and follow-up interviews with 25 organisations, an analysis was conducted that identified five main service clusters....

The EU-Africa PerMed project officially concluded on 31 July 2025, after 4.5 years dedicated to strengthening cooperation between Europe and Africa in personalised medicine (PM)....

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The EOSC4Cancer project officially wrapped up on 31 May....

We are thrilled to share our 2024 Annual Report! 2024 marked the launch of our new Strategic Plan (2024-2027) which builds on all that has come before it and works towards consolidation of the research infrastructure and its activities....

Discover ICTD events our national partners hosted across Europe....

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ISIDORe - Integrated Services for Infectious Disease Outbreak Research, a Horizon Europe-funded project, will conclude its groundbreaking journey on 31 July 2025....

Consulting on strengthening the clinical research and trial ecosystem in the WHO European region....

As part of the COMBINE programme, the European Commission and EU Member States have launched a pilot project to test a new, more efficient way of approving combined studies. These studies involve both clinical trials of medicines and performance studies of medical devices....

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Open Call for Transnational Service Provision: Under the canSERV Open Call researchers are welcome to apply to a portfolio of services offered by canSERV to address the research needs of the entire oncology developmental pipeline....

International Clinical Trials Day (ICTD) was held in Madrid this year alongside our Spanish partners SCReN at Instituto de Salud Carlos III (ISCII). The theme was “Rethinking Clinical Trials: Inclusivity in Practice.”...

The crDSR can hold any type of digital object data sets, documents, media files etc. in a secure research environment....

REMEDI4ALL, Beacon for Rare Diseases and ECRIN co-hosted and a 3-part webinar series that addressed topics such as an introduction to clinical trials, clinical trials for rare diseases and the support and management of clinical trials....

ECRIN has completed deliverable 16.5 within WP16, producing a leaflet which summarises guidelines for data sharing of investigator-initiated clinical studies....

We are excited to announce that registration is now open to join us for International Clinical Trials Day (ICTD) - Rethinking Clinical Trials: Inclusivity in Practice....

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On 27 December 2024 ECRIN and MICYRN signed a Memorandum of Understanding (MoU) with the intention of better aligning their collaboration and capacity to jointly provide operational support to international trials. ...

The revised ACT EU workplan is now available on the ACT EU website, setting out the programme's deliverables and timelines for 2025-2026....

The European public-private partnership consortium MACUSTAR has received a third Letter of Support from the European Medicines Agency (EMA)....

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Thank you to all those who attended our annual CTU Day....

The EU-Africa PerMed project has developed an Action Plan to facilitate, foster, and promote collaboration in Personalised Medicine (PM) between Africa and Europe....

ECRIN is looking forward to joining an ongoing study on "CAtheter-Based Ablation of atrial fibrillation compared to conventional treatment in patients with Heart Failure with Preserved Ejection Fraction". The objective of the study is to assess whether catheter ablation for atrial fibrillation can prevent adverse cardiovascular outcomes i...

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The PERMIT guidelines for designing and implementing all stages of personalised medicine research....

European Life Science Research Infrastructures (LS-RIs)1 work together to benefit the life science community and play a pivotal role in enabling ground-breaking research as part of the ESFRI Roadmap....

Sailing through regulatory hurdles is recognised as one of the toughest challenges in multinational clinical research – RED (Regulatory and Ethical Database), your central resource for navigating the regulatory & ethical landscape for submitting European clinical studies , is here to clear the path....

The aim of SENSITISE is to provide education and training on the importance, conduct and impact of designing clinical trials to ensure appropriate representation of under-served groups....

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The canSERV Consortium is pleased to launch its Specific Call for Service Provision for early career scientists “Training the Next Generation of Cancer Researchers”. ...

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ICRI 2024 for the global research infrastructure community is held in Brisbane, Australia....

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ECRIN is delighted to present its 2023 Annual Report, marking a year filled with significant achievements and highlights. In particular, we were delighted to celebrate our 10 year anniversary since ECRIN was awarded the European Research Infrastructure Consortium (ERIC) status. This report offers an in-depth look at the diverse range of a...

The R-LiNK project wraps-up at the end of this month. This initiative, titled "Optimizing Response to Lithium Treatment through Personalized Evaluation of Individuals with Bipolar Disorder Type I (BDI)," focuses on improving lithium treatment outcomes for BDI patients....

ICTD 2024 brought together stakeholders from the international clinical research community in Thessaloniki (Greece) and online....

We recently issued two updated ECRIN brochures with today’s content in a brand new corporate design....

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