Sponsor & CRO Partnerships

Comprehensive Study Feasibility Request

Share your study requirements with VIGOMED Clinical Trials. This form helps our team evaluate investigator fit, patient access, operational capability, enrollment potential, and start-up readiness.

Preliminary Feasibility

Sponsor / CRO Information

Tell us who is submitting the opportunity and how we can reach you.

Please complete the required fields before continuing:

    1. Sponsor / CRO Information

    Provide the primary contact details for this opportunity.

    2. Study Information

    Share the core study details so we can assess therapeutic and operational alignment.

    3. Patient Population & Enrollment

    Help us understand the target population and expected recruitment commitment.

    4. Study Timeline

    Tell us where the study is in its lifecycle and the timing you need from selected sites.

    5. Operational Requirements

    Select the capabilities required to conduct the study successfully.

    6. Recruitment Requirements

    Share expected enrollment velocity and any recruitment support planned by the sponsor or CRO.

    7. Regulatory & Study Start-Up

    Provide known start-up, IRB, lab, and technology requirements.

    8. Site & Investigator Requirements

    Tell us which investigator qualifications or site characteristics are essential for selection.

    9. Additional Study Information

    Help us understand what matters most in your site selection decision.

    10. Study Documents & Submission

    Upload non-confidential supporting materials and confirm authorization to submit.

    Confidentiality reminder: Please do not upload confidential or proprietary protocol information unless an appropriate CDA/NDA is already in place.
    Suggested: protocol synopsis, feasibility questionnaire, study overview, preliminary inclusion/exclusion criteria, investigator requirements, or recruitment overview.
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