Informed consent type

General Details:

Name:
Informed consent type
Steward:
NINDS
Definition:
Type of informed consent obtained
Registration Status:
Qualified

Permissible Values:

Data Type:
Value List
Unit of Measure:
Ids:
Value Code Name Code Code System Code Description
Written informed consent by the participant/subject Written informed consent by the participant/subject Written informed consent by the participant/subject
Written informed consent by the legal representative on behalf of the participant/subject who gave assent Written informed consent by the legal representative on behalf of the participant/subject who gave assent Written informed consent by the legal representative on behalf of the participant/subject who gave assent
Written informed consent by the legal representative on behalf of the participant/subject who was unable to give assent Written informed consent by the legal representative on behalf of the participant/subject who was unable to give assent Written informed consent by the legal representative on behalf of the participant/subject who was unable to give assent
Waiver of consent Waiver of consent Waiver of consent

Designations:

Designation:
Informed consent type
Tags:

Designations:

Definition:
Type of informed consent obtained
Tags:

Reference Documents:

ID:
Title:
URI:
Provider Org:
Language Code:
Document:
21 CFR 50.20 General requirements for informed consent A Guide to Informed Consent - Information Sheet: Guidance for Institutional Review Boards and Clinical Investigators Contents (http://www.fda.gov/RegulatoryInformation/Guidances/ucm126431.htm#general)

Identifiers:

Source:
NLM
Id:
8rrzSaJw3Gr
Version:
3.1
Source:
NINDS
Id:
C02299
Version:
3
Source:
BRICS Variable Name
Id:
InformConsntTyp
Version: