| Waiver |
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The release from the requirement to obtain informed consent during a study that is granted by Human Subject Protection committee for a research institution for a protocol that is being reviewed by the Institutional Review Board. C103270 |
| Written informed consent by the legal representative on behalf of the participant/subject who gave assent |
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An individual or juridical or other body authorized under applicable law to consent, on behalf of a prospective subject, to the subject's participation in the clinical trial. (ICH): In the same amount or manner; to the same degree; in the role, function, or capacity of.: Someone who takes part in an activity.: Used to indicate that either or both of two items or options may be valid.: A matter or an individual that is observed, analyzed, examined, investigated, experimented upon, or/and treated in the course of a particular study.: Agreement with a statement or proposal to do something.: Printed or written information for future reference.: Consent by a patient to a surgical or medical procedure or participation in a clinical study after achieving an understanding of the relevant medical facts and the risks involved. C142600:C64938:C29867:C48928:C41189:C62281:C86042:C16735(Primary) |
| Written informed consent by the legal representative on behalf of the participant/subject who was unable to give assent |
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An individual or juridical or other body authorized under applicable law to consent, on behalf of a prospective subject, to the subject's participation in the clinical trial. (ICH): In the same amount or manner; to the same degree; in the role, function, or capacity of.: Someone who takes part in an activity.: Used to indicate that either or both of two items or options may be valid.: A matter or an individual that is observed, analyzed, examined, investigated, experimented upon, or/and treated in the course of a particular study.: A response indicating that an individual is unable to do something.: Agreement with a statement or proposal to do something.: Printed or written information for future reference.: Consent by a patient to a surgical or medical procedure or participation in a clinical study after achieving an understanding of the relevant medical facts and the risks involved. C142600:C64938:C29867:C48928:C41189:C121742:C62281:C86042:C16735(Primary) |
| Written informed consent by the participant/subject |
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Someone who takes part in an activity.: Used to indicate that either or both of two items or options may be valid.: A matter or an individual that is observed, analyzed, examined, investigated, experimented upon, or/and treated in the course of a particular study.: Printed or written information for future reference.: Consent by a patient to a surgical or medical procedure or participation in a clinical study after achieving an understanding of the relevant medical facts and the risks involved. C29867:C48928:C41189:C86042:C16735(Primary) |