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Supporting Investigator Sponsored Research

The ISS Program is open to all private practices, hospitals, community health centers, cooperative groups, physician networks, academic medical centers, and universities who are interested in conducting their own research.

An Investigator Sponsored Study (ISS) is one for which the Investigator assumes responsibility for all aspects of the investigation, including:

  • Trial design
  • Ensuring appropriate institutional and regulatory approval
  • Study conduct, including responsibility for ensuring appropriate medical safeguards, medical monitoring, and medical supervision
  • Analysis and interpretation of the results
  • Communication of the results (e.g., publications)

Click here to learn more about becoming a sponsor-investigator.

Teams of medical and scientific staff meet regularly to review investigator sponsored study proposals. Support for these programs is awarded based on scientific merit, patient safety, unmet medical need, availability of funds, and feasibility of the proposal. Teva Pharmaceuticals may provide support for these programs in the form of funding and/or study materials. Funding is dependent upon various factors, including:

  • Availability of funds
  • Merit of the proposal
  • Duration of the proposed study
  • Fair Market Value
All protocols and study activities must comply with, and be conducted pursuant to, Good Clinical Practice (GCP) guidelines and applicable statutes and regulations.

The sponsor-investigator must be qualified and capable of conducting the proposed study in compliance with GCP, applicable federal and local legal requirements, and must not be the subject of any legal restrictions or sanctions.

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In order to expedite your proposal review, we request that all submissions are in English.