ECRIN

ECRIN

TheEuropean Clinical Research Infrastructure Network (ECRIN) is a public, non-profit organisation that links scientific partners and networks across Europe to facilitate multinational clinical research. As of 2013, ECRIN has the legal status of a European Research Infrastructure Consortium (ERIC). ECRIN links the resources and capacities of national networks across Europe to increase access to patients and medical expertise. 

ECRIN’s core office is based in Paris, and ECRIN works with European Correspondents (EuCos) across Europe, national networks of clinical trial units (CTUs)/clinical research facilities (CRFs), as well as numerous European and international stakeholders involved in clinical research.


ECRIN’s organisational model is based on country membership. Countries can either be full Members or Observers. Current Members include Czech Republic, France, Germany, Greece (joined May 2023), Hungary, Ireland, Italy, Norway, Poland, Portugal, Spain and Switzerland (acquired ECRIN member status from being an observer as of June 2023), and Observers include Slovakia. 

Ireland became a full member of ECRIN on November 20th, 2018. As a member of ECRIN, Irish researchers can benefit from a full range of ECRIN services for multinational clinical research study preparation, protocol evaluation and study management.

TheEuropean Clinical Research Infrastructure Network (ECRIN) is a public, non-profit organisation that links scientific partners and networks across Europe to facilitate multinational clinical research. As of 2013, ECRIN has the legal status of a European Research Infrastructure Consortium (ERIC). ECRIN links the resources and capacities of national networks across Europe to increase access to patients and medical expertise. 

ECRIN’s core office is based in Paris, and ECRIN works with European Correspondents (EuCos) across Europe, national networks of clinical trial units (CTUs)/clinical research facilities (CRFs), as well as numerous European and international stakeholders involved in clinical research.

ECRIN’s organisational model is based on country membership. Countries can either be full Members or Observers. Current Members include Czech Republic, France, Germany, Hungary, Ireland, Italy, Norway, Poland, Portugal and Spain, and Observers include Slovakia and Switzerland.  

Ireland became a full member of ECRIN on November 20th, 2018. As a member of ECRIN, Irish researchers can benefit from a full range of ECRIN services for multinational clinical research study preparation, protocol evaluation and study management.

ABOUT Irelands ECRIN Membership

ABOUT Irelands ECRIN Membership

Ireland became a full member of ECRIN on November 20th, 2018.

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As a member of ECRIN, Irish researchers can benefit from a full range of ECRIN services for multinational clinical research study preparation, protocol evaluation and study management

To access ECRIN services contact the Irish EuCos ncto@ucc.ie

To learn more about ECRIN, please see the video below

PROPOSAL DEVELOPMENT STAGE

ECRIN can offer more extensive support during the proposal development stage when it is involved as a project partner. Support may be required for EU funding proposals such as Horizon Europe and Innovative Health Initiative (IHI). Researchers should contact the Irish EuCos early in the proposal development process (ideally 3 to 6 months prior to the submission deadline).

PROPOSAL DEVELOPMENT STAGE

ECRIN can offer more extensive support during the proposal development stage when it is involved as a project partner. Support may be required for EU funding proposals such as Horizon Europe and Innovative Health Initiative (IHI). Researchers should contact the Irish EuCos early in the proposal development process (ideally 3 to 6 months prior to the submission deadline).

Examples of the types of support available at the proposal stage include:

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Design and methodology support

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Advice on EU funding sources

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Budget development and cost estimation

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Regulatory, ethics and insurance requirements

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Medical expertise and support

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Strategies for site selection and patient recruitment

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Design and methodology support

icon of the globe

Advice on EU funding sources

a stack of books icon

Budget development and cost estimation

A clipboard with a checkmark icon

Regulatory, ethics and insurance requirements

Four squared pattern icon

Medical expertise and support

a circle with a checkmark icon

Strategies for site selection and patient recruitment

POST FUNDING AWARD – STUDY PREPARATION

Once the study has been awarded funding ECRIN can provide the following support during the study preparation phase:

POST FUNDING AWARD – STUDY PREPARATION

Once the study has been awarded funding ECRIN can provide the following support during the study preparation phase:

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Protocol peer review

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Feasibility and risk assessment

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Protocol peer review

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Feasibility and risk assessment

STUDY IMPLEMENTATION

ECRIN offers support during the study implementation phase in various areas such as:

STUDY IMPLEMENTATION

ECRIN offers support during the study implementation phase in various areas such as:

Study management and coordination

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Regulatory and ethical submissions

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Selection and provision of qualified resources

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Pharmacovigilance (adverse event reporting)

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Data management

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Monitoring

Study management and coordination

A noteboard icon

Regulatory and ethical submissions

A checkmark icon

Selection and provision of qualified resources

An up arrow graph icon

Pharmacovigilance (adverse event reporting)

A checkboard icon

Data management

A graph board icon

Monitoring