Internal portal

COPRI data request form

Researchers responsible for the data request must:

  • Comply with Quebec’s rules regarding confidentiality and respect for privacy.
  • The transferred data will be anonymized (triple coding), containing no information that could identify the participants. All presented data must be in such a way that no patient can be identified.
  • The responsible researchers must understand that the data is the property of the RI-MUHC and must obtain approval from the COPRI Data Access Committee to proceed with the analyses described in the request. Additional analyses cannot be conducted without the committee’s approval, and the results should only be disseminated in the contexts described in the request.
  • The inclusion and order of authors must adhere to the authors listed in the data request and the COPRI authorship policy.
  • Once the data request project is completed, which is typically the publication of the manuscript, the shared database must be destroyed by the responsible researcher, and a written, dated, and signed confirmation to that effect must be sent to the cohort director.

Any use of data from COPRI requires approval of a data request by the Data Access Committee. Please refer to the Data Management Policy, and the COPRI Authorship Policy which you must follow for any work using COPRI data. An electronic version of this form will be available on the COPRI website. If the electronic version does not work, please send your request to the COPRI director by email: alexandra.depokomandy@mcgill.ca.

    Merci pour votre intérêt. Vous pouvez contacter l’équipe COPRI sur info@copri.ca

    Veuillez remplir le formulaire pour évaluation par le Comité d’accés aux données COPRI

    Co-auteurs/co-authors

    Raison de la requête / Reason for request

    Quelle conférence scientifique ? / Which scientific conference?

    Date limite pour la soumission / Deadline for submission

    Avez-vous obtenu l’approbation éthique ? / Do you have ethical approval ?

    Brève description du projet. Inclure rationale, objectifs, inclusions/exclusions, définition des issues primaires et des autres variables, plan d’analyses.
    Brief description of project. Include rationale, objectives, inclusions/exclusions, outcome and covariate definitions, analysis plan.

    Si disponible, joindre le protocole à cette requête / If available, attach protocol to this request

    Source des données requises / Source of requested data

    Sélectionnez les cliniques / Select which clinics
    CLSC Côte-des-NeigesGMF-U HerzlCLSC Parc-ExtensionGMF-U Vallée-de-l’OrGMF-U St. Mary’sGMF-U GatineauGMF-U Jardins-Roussillon

    Type de données requises / Type of data required

    Les données des DMÉ seront disponibles bientôt / EMR data will be available soon

    Voir dictionnaire de données Questionnaire Cycle 1

    Sélectionnez le type de donnée du questionnaire cycle 1

    This form uses Akismet to reduce spam. Learn how your data is processed.

    EN
    EN FR