Clinical Trial Informed Consent
Research participation agreement explaining study procedures, potential risks, benefits, and participant rights. Includes withdrawal options, compensation details, and informed consent requirements for medical research.
Key Clauses
Purpose and Scope
Clearly defines the arrangement, transaction, or service being agreed upon between the parties.
Rights and Obligations
Details the specific responsibilities and entitlements of each party under the agreement.
Liability and Risk
Addresses assumption of risk, liability limitations, and hold harmless provisions.
Payment Terms
Specifies amounts due, payment methods, refund policies, and any additional cost responsibilities.
Termination
Establishes conditions and procedures for ending the agreement, including notice requirements.
Use This Template
When You Need This
- Cancer patient participating in experimental treatment research study
- Volunteer joining pharmaceutical drug testing for new medication
- Patient enrolling in medical device trial for innovative treatments
- Research participant in behavioral health or psychology study