Broad consent definition

Broad consent means the donor donates materials with permission to use them for a broad range of future studies, subject only to further prior ethics review and approval
Sample 1Sample 2Sample 3
Broad consent means the details of new research in the future are not precisely specified in the information for research subjects. It is consent that does not define the exact nature of future work but may indicate the areas of interest”.
Sample 1
Broad consent means the details of new research in the future are not precisely specified in the information for research subjects.)
Sample 1

Examples of Broad consent in a sentence

  • Broad consent may be obtained in lieu of informed consent obtained in accordance with paragraphs (b) and (c) of this section only with respect to the storage, maintenance, and secondary research uses of identifiable private information and identifiable biospecimens.

  • Broad consent for the storage, maintenance, and secondary research use of identifiable private information or identifiable biospecimens (collected for either research studies other than the proposed research or nonresearch purposes) is permitted as an alternative to the informed consent requirements in paragraphs (b) and (c) of this section.

  • Broad consent shall only be used in VA research when identifiable data or biospecimens are collected solely for research purposes.

  • Broad consent may be obtained in lieu of informed consent obtained in accordance with paragraphs (b) and (c) of this section only with respect to the storage, maintenance, and secondary re- search uses of identifiable private informa- tion and identifiable biospecimens.

  • Broad consent for the storage, maintenance, and secondary research use of identifiable private information or identifiable biospecimens (collected for either research studies other than the proposed research or nonresearch purposes) is permitted as an alternative to the informed consent requirements in paragraphs B and C of this section.

  • Broad consent for the storage, maintenance, and secondary research use of identifiable private information or identifiable biospecimens (collected for either research studies other than the proposed research or nonresearch purposes) is permitted under the revised Common Rule.

  • Broad consent may be obtained in lieu of informed consent obtained in accordance with section B of this section only with respect to the storage, maintenance, and secondary research uses of identifiable private information and identifiable biospecimens.

  • Broad consent is permitted under the Revised Common Rule and may be obtained in lieu of informed consent in accordance with the basic and additional elements of consent, but only with respect to the storage, maintenance, and secondary research use of identifiable private information or identifiable biospecimens (collected for either research studies other than the proposed research or non-research purposes).

  • The requirement for written consent may be waived under one of the following conditions: • the research involves no or only minimal risk• the consent form will be the only evidence linking the subject and the research, and the primary risk of harmis to the subject’s privacy Broad consent may be obtained in lieu of informed consent for the storage, maintenance, and secondary research uses of identifiable private information.

  • Broad consent from the participants will be sought for storage of blood and other specimens, such as saliva and urine where applicable, and for future use by researchers according to the Node’s scientific strategy.

Related to Broad consent

  • Informed consent means a documented written agreement to allow a proposed action, treatment, or service after full disclosure provided in a manner the individual or his or her guardian understands, of the relevant facts necessary to make the decision. Relevant facts include the risks and benefits of the action, treatment, or service; the risks and benefits of the alternatives to the action, treatment, or service; and the right to refuse the action, treatment, or service. The individual or his or her guardian, as applicable, may revoke informed consent at any time.

  • Required Consents shall have the meaning set forth in Section 4.5.