North Carolina 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 North Carolina Specimen Repository Agreement is a legal contract established within the healthcare and research industry to define the guidelines and procedures for the collection, storage, and utilization of biological specimens within the state of North Carolina. This agreement is specifically designed to safeguard the rights of individuals whose specimens are collected, ensuring their privacy, confidentiality, and informed consent. The main purpose of the North Carolina Specimen Repository Agreement is to facilitate medical research and discovery by allowing researchers and healthcare providers access to securely stored biological samples. By implementing this agreement, North Carolina aims to enhance scientific advancements, improve medical treatments, and ultimately advance public health. This agreement sets out specific terms and conditions that must be adhered to by all parties involved, including healthcare institutions, researchers, and specimen donors. It is crafted to ensure ethical and legal standards are met throughout the process of specimen collection, storage, sharing, and analysis. The North Carolina Specimen Repository Agreement specifies the following key components: 1. Informed Consent: This outlines the establishment of a clear and transparent process whereby individuals provide consent for the collection and usage of their biological specimens for specific research purposes. It ensures that individuals are fully aware of the intended usage of their specimens before giving their consent. 2. Confidentiality and Privacy: This section guarantees the protection of individuals' privacy and ensures that their identifiable information remains confidential throughout the process. It highlights the importance of maintaining strict security measures to prevent unauthorized access or disclosure of sensitive data. 3. Ownership and Use: This component addresses the ownership rights of collected specimens and specifies how they can be used for research purposes. It clarifies whether ownership remains with the donor, is transferred to the repository, or is shared jointly between the parties involved. 4. Access and Sharing: The agreement outlines the policies and procedures regarding access to the specimen repository for authorized researchers and institutions. It establishes guidelines for sharing specimens, data, and research findings while maintaining the privacy and confidentiality of individuals. 5. Withdrawal and Disposal: This section defines the process through which individuals can withdraw their consent and request the removal or disposal of their specimens from the repository. It highlights the responsibilities of the repository in such instances, ensuring compliance with the donor's wishes. While there may not be different types of North Carolina Specimen Repository Agreements, it is crucial to note that the agreement can be customized to suit the specific needs and requirements of different institutions, research programs, or initiatives within the state. These adaptations may involve additional clauses or provisions to address unique circumstances or research focus areas, all while still aligning with the overarching principles and legal standards set forth by the state of North Carolina.

The North Carolina Specimen Repository Agreement is a legal contract established within the healthcare and research industry to define the guidelines and procedures for the collection, storage, and utilization of biological specimens within the state of North Carolina. This agreement is specifically designed to safeguard the rights of individuals whose specimens are collected, ensuring their privacy, confidentiality, and informed consent. The main purpose of the North Carolina Specimen Repository Agreement is to facilitate medical research and discovery by allowing researchers and healthcare providers access to securely stored biological samples. By implementing this agreement, North Carolina aims to enhance scientific advancements, improve medical treatments, and ultimately advance public health. This agreement sets out specific terms and conditions that must be adhered to by all parties involved, including healthcare institutions, researchers, and specimen donors. It is crafted to ensure ethical and legal standards are met throughout the process of specimen collection, storage, sharing, and analysis. The North Carolina Specimen Repository Agreement specifies the following key components: 1. Informed Consent: This outlines the establishment of a clear and transparent process whereby individuals provide consent for the collection and usage of their biological specimens for specific research purposes. It ensures that individuals are fully aware of the intended usage of their specimens before giving their consent. 2. Confidentiality and Privacy: This section guarantees the protection of individuals' privacy and ensures that their identifiable information remains confidential throughout the process. It highlights the importance of maintaining strict security measures to prevent unauthorized access or disclosure of sensitive data. 3. Ownership and Use: This component addresses the ownership rights of collected specimens and specifies how they can be used for research purposes. It clarifies whether ownership remains with the donor, is transferred to the repository, or is shared jointly between the parties involved. 4. Access and Sharing: The agreement outlines the policies and procedures regarding access to the specimen repository for authorized researchers and institutions. It establishes guidelines for sharing specimens, data, and research findings while maintaining the privacy and confidentiality of individuals. 5. Withdrawal and Disposal: This section defines the process through which individuals can withdraw their consent and request the removal or disposal of their specimens from the repository. It highlights the responsibilities of the repository in such instances, ensuring compliance with the donor's wishes. While there may not be different types of North Carolina Specimen Repository Agreements, it is crucial to note that the agreement can be customized to suit the specific needs and requirements of different institutions, research programs, or initiatives within the state. These adaptations may involve additional clauses or provisions to address unique circumstances or research focus areas, all while still aligning with the overarching principles and legal standards set forth by the state of North Carolina.