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Consent And Indemnity Form
"I need a Consent and Indemnity Form for a medical research study in Lagos, Nigeria, where we'll be collecting blood samples from adult participants over a 6-month period starting March 2025, with specific emphasis on data protection and medical risk disclosure."
1. Parties: Identification of all parties involved - the person/entity giving consent and being indemnified, and the person/entity receiving consent and indemnification
2. Background: Brief context explaining the purpose of the consent and indemnity arrangement
3. Definitions: Clear definitions of key terms used throughout the document
4. Scope of Consent: Detailed description of the specific activities, uses, or rights being consented to
5. Acknowledgment of Risks: Clear statement of risks involved and confirmation that these have been understood
6. Indemnification Provisions: Specific terms of indemnification including scope, limitations, and duration
7. Representations and Warranties: Statements confirming the person giving consent has the capacity and authority to do so
8. Duration and Termination: Period for which the consent and indemnity remain valid and any termination conditions
9. Governing Law: Confirmation that Nigerian law governs the agreement
10. Execution: Signature blocks and execution requirements
1. Medical Disclosure: Additional section for medical-related consent forms, including medical history and specific health-related risks
2. Data Protection Provisions: Required when personal data processing is involved, ensuring compliance with NDPR 2019
3. Parent/Guardian Consent: Required when the subject is a minor or lacks capacity to give consent
4. Insurance Details: When relevant insurance coverage needs to be specified
5. Emergency Contacts: For activities where emergency contact information might be needed
6. Dispute Resolution: Optional alternative dispute resolution mechanisms before court proceedings
7. Severability: Clause ensuring survival of remaining provisions if some are found invalid
1. Schedule 1 - Activity Details: Detailed description of the specific activities or services covered by the consent
2. Schedule 2 - Risk Disclosure: Comprehensive list of potential risks and their implications
3. Schedule 3 - Medical Information Form: For medical-related consents, detailed medical information collection form
4. Appendix A - Emergency Procedures: Relevant emergency procedures and protocols where applicable
5. Appendix B - Insurance Coverage Details: Detailed information about relevant insurance coverage and limits
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