Teva - Data Request Portal

Teva - Data Request Portal

Teva is committed to supporting clinical trial disclosure and responsible data sharing in compliance with global legal and regulatory requirements and in alignment with the biopharmaceutical industrys principles.

To learn more about Teva's Clinical Trial Transparency policy.

  1. New users need to register for a new account
  2. When you are ready to submit a Data Request, please have the following information ready:
    • Research Objective
    • Scientific Rationale
    • Research Questions/Hypothesis
    • Primary Endpoint (if applicable)
    • Secondary Endpoint(s) (if applicable)
    • Program(s) Requested
    • Studies Requested
    • Description of Data REquested
    • Description of Variables Requested (optional)
    • Publication Plan
    • Summary of Analysis Plan
    • Funding of Proposed Research
    • Potential Conflict(s) of Interest
    • Management Plan for Conflicts of Interest
    • Statistical Analysis Plan
    • IRB Approval

In order to submit a request for clinical trial data, please follow the steps below:

  • Log in to the system with your user credentials
  • Select New Request from the left navigation panel
  • Complete the Data Request form and submit the request

Note: You will be required to complete all entries of the form, which will take approximately 15-30 minutes. Please compile all required information before you begin. All information must be completed before you can submit. If you have any questions, please contact

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