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WASABI model CRO CIA 2014 ScotlandTRIPARTITE CLINICAL INVESTIGATION AGREEMENT FOR MEDICAL TECHNOLOGY INDUSTRY SPONSORED RESEARCH IN SCOTTISH HEALTH BOARDS, MANAGED BY CONTRACT RESEARCH Organizations

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What is tripartite clinical investigation agreement?

The tripartite clinical investigation agreement is a legal document that outlines the responsibilities and obligations of three parties involved in a clinical investigation - the sponsor, the investigator, and the institution.

Who is required to file tripartite clinical investigation agreement?

The sponsor of the clinical investigation is required to file the tripartite clinical investigation agreement.

How to fill out tripartite clinical investigation agreement?

The tripartite clinical investigation agreement can be filled out by including all relevant information about the sponsor, investigator, and institution, as well as detailing the responsibilities and obligations of each party.

What is the purpose of tripartite clinical investigation agreement?

The purpose of the tripartite clinical investigation agreement is to ensure that all parties involved in the clinical investigation are aware of their responsibilities and obligations, and to protect the rights and well-being of the subjects participating in the study.

What information must be reported on tripartite clinical investigation agreement?

The tripartite clinical investigation agreement must include information about the sponsor, investigator, institution, study protocol, funding source, and any potential conflicts of interest.

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