Tennessee Specimen Repository Agreement

• Category: Corporations - Public
• State: Multi-State
• Control #: US-EG-9160
• Format: Word; Rich Text

Description

DNA Specimen Repository Agreement between The University of North Texas Health Science Center at Forth Worth and GeneLink, Inc. dated June 21, 1995. 12 pages The Tennessee Specimen Repository Agreement is a legal document that outlines the terms and conditions governing the collection, storage, and use of biological specimens in the state of Tennessee. It serves as a contract between the specimen donors and the repository, ensuring the proper handling and confidential storage of donated specimens for research or clinical purposes. Key terms included in the Tennessee Specimen Repository Agreement are: 1. Specimen Donor: The individual or entity who provides the biological specimen(s) to the repository for storage and potential research use. 2. Specimen Repository: The organization responsible for collecting, receiving, storing, and managing the biological specimens. 3. Informed Consent: The voluntary agreement of the specimen donor to contribute their specimen(s) for research or clinical purposes after being informed about the nature and objectives of the repository. 4. Confidentiality: The agreement ensures that the personal information and identity of the specimen donor are protected and kept confidential. 5. Ownership and Use of Specimens: This section outlines the ownership of the donated specimens, usually stating that once donated, the specimens become the property of the repository. It also details how the specimens will be used in research and whether any commercial interests may arise from their use. 6. Withdrawal of Consent: Specifies the conditions under which a specimen donor can withdraw their consent for the use of their specimen(s) and outlines the process for the removal or destruction of the specimen(s) from the repository. 7. Ethical Considerations: The agreement may address ethical considerations such as ensuring the protection of vulnerable populations, obtaining approval from relevant ethics committees, and complying with legal and regulatory requirements. Different types of Tennessee Specimen Repository Agreements may include: 1. Medical Research Repository Agreement: This agreement is specifically designed for the collection and storage of specimens for medical research purposes, such as discovering new treatments, studying diseases, or advancing medical knowledge. 2. Clinical Repository Agreement: This agreement focuses on the collection and storage of specimens for clinical purposes, such as diagnostic testing, monitoring treatment effectiveness, or conducting genetic research to provide personalized care. 3. Genetic Repository Agreement: This type of agreement pertains to the collection and storage of biological specimens for genetic research, including genotypic, genome sequencing, or identification of genetic markers for various conditions. 4. Population Health Repository Agreement: This agreement aims to collect and store specimens for population-level studies, epidemiological research, or tracking public health trends. In conclusion, the Tennessee Specimen Repository Agreement is a comprehensive legal document that governs the storage, use, and ethical considerations concerning biological specimens donated for research or clinical purposes. It ensures the protection of donor privacy, ownership rights, and outlines the various types of agreements that can be specific to different research or clinical objectives.

The Tennessee Specimen Repository Agreement is a legal document that outlines the terms and conditions governing the collection, storage, and use of biological specimens in the state of Tennessee. It serves as a contract between the specimen donors and the repository, ensuring the proper handling and confidential storage of donated specimens for research or clinical purposes. Key terms included in the Tennessee Specimen Repository Agreement are: 1. Specimen Donor: The individual or entity who provides the biological specimen(s) to the repository for storage and potential research use. 2. Specimen Repository: The organization responsible for collecting, receiving, storing, and managing the biological specimens. 3. Informed Consent: The voluntary agreement of the specimen donor to contribute their specimen(s) for research or clinical purposes after being informed about the nature and objectives of the repository. 4. Confidentiality: The agreement ensures that the personal information and identity of the specimen donor are protected and kept confidential. 5. Ownership and Use of Specimens: This section outlines the ownership of the donated specimens, usually stating that once donated, the specimens become the property of the repository. It also details how the specimens will be used in research and whether any commercial interests may arise from their use. 6. Withdrawal of Consent: Specifies the conditions under which a specimen donor can withdraw their consent for the use of their specimen(s) and outlines the process for the removal or destruction of the specimen(s) from the repository. 7. Ethical Considerations: The agreement may address ethical considerations such as ensuring the protection of vulnerable populations, obtaining approval from relevant ethics committees, and complying with legal and regulatory requirements. Different types of Tennessee Specimen Repository Agreements may include: 1. Medical Research Repository Agreement: This agreement is specifically designed for the collection and storage of specimens for medical research purposes, such as discovering new treatments, studying diseases, or advancing medical knowledge. 2. Clinical Repository Agreement: This agreement focuses on the collection and storage of specimens for clinical purposes, such as diagnostic testing, monitoring treatment effectiveness, or conducting genetic research to provide personalized care. 3. Genetic Repository Agreement: This type of agreement pertains to the collection and storage of biological specimens for genetic research, including genotypic, genome sequencing, or identification of genetic markers for various conditions. 4. Population Health Repository Agreement: This agreement aims to collect and store specimens for population-level studies, epidemiological research, or tracking public health trends. In conclusion, the Tennessee Specimen Repository Agreement is a comprehensive legal document that governs the storage, use, and ethical considerations concerning biological specimens donated for research or clinical purposes. It ensures the protection of donor privacy, ownership rights, and outlines the various types of agreements that can be specific to different research or clinical objectives.