Αποτελέσματα Αναζήτησης
A waiver of documentation of informed consent (waiver of the requirement for a signature on a consent form) can be obtained under certain circumstances by the Investigator: The study involves only minimal risk and the research does not include any procedures for which written consent is required.
30 Δεκ 2021 · The HIPAA waiver of authorization allows doctors to provide information on a patient’s health to third parties, such as researchers, attorneys, other doctors or family members.
2 Φεβ 2024 · Under the HIPAA Privacy Rule, an institutional review board (IRB) or privacy board must approve a waiver or alteration of authorization. Specifically, the following must be documented:
21 Σεπ 2020 · Michigan Medicine study teams request waivers and alterations of HIPAA authorization through eResearch Regulatory Management application sections 25-1 (select the box for waiver) and 25-2 (complete the waiver request).
A covered entity may use or disclose protected health information for research purposes pursuant to a waiver of authorization by an IRB or Privacy Board, provided it has obtained documentation of all of the following: Identification of the IRB or Privacy Board and the date on which the alteration or waiver of authorization was approved;
The HIPAA waiver is allowed under the HIPAA Privacy Rule. It is a legal document that permits covered entities to use or disclose a patient’s protected health information (PHI), without individual authorization, to a third party when meeting specific conditions (1).
23 Ιουλ 2021 · IRB must always approve a waiver of documentation of consent and, where appropriate, an alteration of authorization if the investigator will not obtain a consent form signed and dated by the research participant.
