Collaboration Request

CRO

    Information

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    Study

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    Documents

    The attaches for this section are optional. Formats .jpg, .png, .pdf up to 2 MB.

    Approval by the competent Ethics Commission

    Informed Consent Form

    Clinical Research Protocol

    Principal Investigator’s Curriculum Vitae

    Authorization Statement From the Service Director

    Insurance

    Clinical Study Agreement

    Statement of Responsibility

    As Principal Investigator, I declare in my honor that the information provided is true. I further declare that the clinical research protocol and all the scientific papers presented within the scope of this clinical study will make specific reference to the source of support (Clinical Academic Center of Braga (2CA-Braga)).