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Medtech Translate Membership

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  • If you wish to apply as a expert/advisory member you will be asked to upload your CV as part of the signup process. For further information on MedTechTranslate privacy, data protection and retention policies please
  • Standard Membership

    Become a Medtech Translate member to access ‘stage-of-development’ guidance and information resources designed and developed to help you, the device developer, navigate and understand many complex requirements for bringing a device to market.

    In addition to the guidance and information provided through the portal standard membership benefits also include access to the Medtech Translate device development support programme whereby standard members can request the input, advice or support of clinical advisory members who have expressed an interest in, or experience of, supporting medical device development, research translation or trials.

    On application you will be asked to provide your contact details and some additional background information relevant to the MedTechTranslate portal and its remit.

    Your curriculum vitae is not required on application .

    Clinical advisory

    If you have an interest in, or previous experience of, supporting medical device development or research translation you can, in addition to availing of standard MedTechTranslate membership, also elect to participate in the Medtech Translate device development support programme. This programme is designed to assist and support any Medtech Translate member requiring clinical input and/ or advice to their device development project.

    Clinical advisory members get all the benefits of MedTechTranslate membership. However, by agreeing to become a Medtech Translate advisory member you are indicating your willingness to examine requests for advice or input from standards members and that you are open to being contacted by us in this regard.

    Clinical advisory +

    Advisory membersare also eligible to participate, through our association with HRB-CRCI, in the HRB-CRCI National Study Feasibility Programme. Study feasibility is a process through which a clinical trial sponsor identifies potential investigator sites and evaluates if they are suitable to conduct a clinical trial or investigation.

    On application, you will be asked to provide your contact details as well as some additional background information (relevant to Medtech Translate and the HRB CRCI feasibility programme), including your curriculum vitae (to allow us confirm your eligibility) as well as your areas of clinical interest.

    OAll information gathered is relevant to the MedTechTranslate portal and its remit and will be shared with HRB – CRCI as appropriate.

    For more information on HRB-CRCI please visit their website at: https://www.hrb-crci.ie

  • Sector Information

    Please indicate your institutional and professional body affiliations by filling in or ticking all boxes relevant to you below

  • Member Experience

    (Device development / Regulatory / Clinical Trials)

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  • We ask you to select your areas of clinical / research interest. This will enable us to support and administer the MedTechTranslate expert / advisory function.

  • Clinical trials/Investigations Experience

    Please fill in the form below indicating your experience of clinical trials/investigations to date:

  • If you have a clinical background and have an interest in partaking in, or supporting medical device clinical trials, you might also consider joining the HRB-CRCI National Study Feasibility Programme
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Medtech Translate

CRDI / CÚRAM Partnership Project
Clinical Research Development Ireland,
28 Upper Mount Street,
Dublin 2, Ireland
Ph: 01 – 658 2135
Email: medtechtranslate@crdi.ie

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The guidance and information accessible through Medtech Translate has been prepared by the CRDI / CÚRAM partnership project to help users understand EU medical device regulatory requirements. It is intended to be general guidance for education and informational purposes only. It is not legal advice.