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Central Adelaide Local Health Network
Research OfficeClinical Research Agreement Guidelines
1. Introduction
Each clinical trial to be conducted at a site within SA Health and sponsored by a third
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What is clinical research agreement guidelines?
Clinical research agreement guidelines are a set of rules and regulations that govern the collaboration between sponsors, investigators, and institutions involved in clinical research studies.
Who is required to file clinical research agreement guidelines?
All parties involved in a clinical research study, including sponsors, investigators, and institutions, are required to follow and file clinical research agreement guidelines.
How to fill out clinical research agreement guidelines?
Clinical research agreement guidelines are typically filled out by the principal investigator or designated representative, following the instructions provided by the sponsoring institution or organization.
What is the purpose of clinical research agreement guidelines?
The purpose of clinical research agreement guidelines is to provide a framework for ensuring compliance with ethical, legal, and regulatory requirements in the conduct of clinical research studies.
What information must be reported on clinical research agreement guidelines?
Clinical research agreement guidelines typically require information such as study objectives, protocols, responsibilities of parties involved, financial disclosures, and data sharing agreements.
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