Clinical Trial Agreement Template India

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PandaTip: Sponsors of clinical trials often provide equipment or other assets, in addition to financial support. In this section of the model, you can describe in detail all the materials that the sponsor will provide during the clinical trial. PandaTip: The above table of contents in this template makes it easy to navigate through the different sections of the Clinical Trials Agreement. Both the institution and the sponsor fully agree to the transmission and exchange of confidential information through the study. Both Parties agree that, for the duration of this Clinical Trials Agreement and for a period of five years from the conclusion of this Agreement, both Parties shall maintain that all services provided by the Sponsor remain the property of the Sponsor during and after the conclusion of the Study. PandaTip: Clinical trials often publish their results in scientific journals and other publications. This section of this document describes the conditions for the publication of clinical trial results. An investigator`s Undertaking is one of the documents submitted to the Central Drugs Standard Control Organization (CDSCO) requesting permission to conduct a clinical trial in India (along with other documents). The UI is a supportive legal document in which the auditor undertakes to conduct the study in accordance with applicable regulatory, ethical and good clinical practice guidelines. . .

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