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1. Parties: Identifies all parties to the agreement, including the research sponsor, clinical site, and principal investigator
2. Background: Outlines the purpose of the clinical study and the parties' intentions
3. Definitions: Defines key terms used throughout the agreement
4. Scope of Services: Details the clinical services to be provided and study requirements
5. Compliance Requirements: Outlines regulatory compliance obligations including GCP, IRB approval, and protocol adherence
6. Payment Terms: Specifies payment schedule, amounts, and conditions for payment
7. Confidentiality: Details handling of confidential information and data protection requirements
8. Term and Termination: Specifies agreement duration and termination conditions
1. Equipment and Supplies: Details provision and handling of study equipment - include when sponsor provides equipment or supplies for the study
2. Subject Injury: Provisions for handling research-related injuries - include when study involves human subjects with injury risks
3. Publication Rights: Terms for publishing study results - include when academic institutions are involved or publication rights are important
1. Protocol: Detailed study protocol and methodology
2. Budget: Detailed payment schedule and cost breakdown
3. Payment Schedule: Timeline and conditions for payments
4. Required Documentation: List of required regulatory documents and certifications
5. Data Protection Requirements: Specific data handling and protection procedures
6. Insurance Certificates: Proof of required insurance coverage
Find the exact document you need
Clinical Agreement
A U.S.-governed agreement establishing terms for clinical services or research, ensuring compliance with healthcare regulations and standards.
Clinical Site Agreement
A U.S.-governed agreement between research sponsors and clinical sites for conducting clinical trials, ensuring regulatory compliance and defining operational terms.
Data Transfer Agreement Clinical Trial
A U.S.-compliant agreement governing the transfer of clinical trial data between parties, ensuring regulatory compliance and data protection.
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