№ lp_1_2_46813
File format: docx
Character count: 47422
File size: 114 KB
Institutional informed consent template outlining required language, structure, and regulatory context for enrolling adult and minor participants in minimal risk human research studies.
Document type:
Informed consent form template
Research category:
Human subjects research
Risk level:
Minimal risk
Governing standards:
Institutional Review Board requirements; Associated Press Style Manual
Regulatory references:
U.S. Food and Drug Administration
Responsible organization:
Jaeb Center for Health Research IRB
Intended institutions:
Academic medical centers and affiliated health systems
Target audience:
Research participants and legally authorized representatives
Geographic context:
United States
Source type:
Institutional research ethics documentation
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2023
Region / city:
Belgium
Topic:
Legal and technical elements of an invoice
Document type:
Invoice
Organization:
Belgian VAT regulation authority
Author:
N/A
Target audience:
Companies and service providers in Belgium
Period of validity:
N/A
Approval date:
N/A
Amendment date:
N/A
Year:
2022
Month:
August
Document type:
Guidance and standardized study document
Subject:
Biological resources and environmental analysis
Issuing body:
California Department of Transportation
Division:
Division of Environmental Analysis, Office of Biological Studies
Jurisdiction:
State of California
Applicable programs:
State Highway System projects
Related standards:
Standard Environmental Reference (SER)
Compliance references:
Americans with Disabilities Act
Advisory group:
Biological Consultancy Group
Intended projects:
Minor A and B transportation projects with limited natural resource impacts
Preparation requirements:
Associate Environmental Planner (Natural Science) or equivalent
Source type:
Government technical guidance document
Year:
2023
Region / City:
Australia
Topic:
Mental Health Treatment Plan
Document Type:
Medical Form
Institution:
Medicare Australia
Author:
Unknown
Target Audience:
Healthcare Providers, General Practitioners
Validity Period:
From date of creation until the next review
Approval Date:
Not specified
Modification Date:
Not specified
Contextual Description:
A medical form detailing the minimal requirements for a GP mental health treatment plan, including patient information, assessment, interventions, and consent for sharing health data.
Note:
Year
Year:
2026
Region / City:
Palo Alto, Stanford
Topic:
Research Consent Template
Document Type:
Consent Form
Organization:
VA Palo Alto, Stanford University
Author:
VA Palo Alto Research Team
Target Audience:
Research Participants
Duration of Study:
Varies
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Subject:
Research Ethics
Document Type:
Template
Organization:
Medical College of Wisconsin
Target Audience:
Research participants
Institution:
University of British Columbia
Document type:
Clinical informed consent form template
Study risk level:
Minimal risk
Regulatory scope:
Not regulated by Health Canada or the U.S. Food and Drug Administration
Jurisdiction:
British Columbia, Canada
Intended use:
Non-regulated clinical research studies
Target audience:
Research participants from the general population
Reading level:
Grade 7
Applicable populations:
Adults and, where applicable, pediatric participants with parental permission and child assent
Ethics oversight:
Research Ethics Board (REB)
Source type:
Institutional research ethics documentation
Note:
Year
Topic:
Research Ethics
Document Type:
Consent Notice
Organization / Institution:
San Jose State University
Author:
Lisa Simpson, San Jose State University graduate student
Target Audience:
Participants in minimal risk research involving adults
Contextual Description:
A consent notice for a minimal risk research study involving adults, explaining participant rights, study procedures, and confidentiality measures.
Note:
Authors
Website:
http://www.aamt.info/english/utx/
Status:
official release
Last updated:
March 19, 2019
Document language:
English
License:
CC0 1.0
Disclaimer:
See http://aamt.info/english/utx/index.htm#disclaimer
File structure:
tab-delimited text
File extension:
".utx"
Character encoding:
UTF-8 with BOM.
New line code:
"
" (CR+LF).
Line comment symbol:
# (hash symbol).
UTX version:
1.20
User-defined fields:
x-termUsage:en
Type of document:
Institutional research guideline
Subject:
Verbal informed consent procedure
Applicable to:
Minimal risk research
Reviewing body:
Institutional Review Board (IRB)
Institution mentioned:
Governors State University
Content elements:
Consent requirements, participant protections, sample scripts
Consent format:
Verbal consent in lieu of written consent
Required components:
Research description, procedures, duration, confidentiality, investigator contact information
Associated materials:
Written invitation, information sheet, verbal consent script
Program Name/Jurisdiction:
Maryland Breast and Cervical Cancer Program and/or CRF Cancer Prevention, Education, Screening and Treatment Program
Fiscal Year:
2024
Document Type:
Administrative standards and eligibility guidelines
Geographic Scope:
Maryland, United States
Administering Authority:
Local Maryland cancer screening programs
Subject:
Eligibility criteria for screening, diagnostic, referral, and treatment services
Target Population:
Maryland residents seeking cancer screening and related services
Eligibility Criteria:
Residency, annual gross household income up to 250% of Federal Poverty Level, family size, insurance status
Verification Requirements:
Verbal or written proof of residency, income documentation, insurance verification, Medicaid status confirmation via EVS
Programs Referenced:
BCCP-CPEST Programs, Patient Navigation Only (PNO), Cancer Screening and Tracking (CaST), Client Database (CDB)
Standards Referenced:
Minimal Clinical Elements (MCE), Minimal Standards for Nursing Case Management
City of Alliance Notice on Minimal Staffing at City Hall Due to Inclement Weather, December 13, 2021
Date:
December 13, 2021
City:
Alliance, Nebraska
Country:
United States
Organization:
City of Alliance
Department:
City Hall
Document Type:
Press Release
Topic:
Inclement Weather and Municipal Operations
Audience:
Residents and service users of the City of Alliance
Operational Status:
Minimal staffing at city hall
Contact Phone:
(308) 762-4955
Website:
www.cityofalliance.net
Distribution Status:
For Immediate Release
Year:
2022
Region / City:
United Kingdom
Topic:
Subsidy Control
Document Type:
Form
Organization / Institution:
Department for Energy Security and Net Zero (DESNZ)
Author:
Salix
Target Audience:
Enterprises applying for PSDS grants
Effective Period:
Current and two most recent financial years
Approval Date:
Not specified
Modification Date:
Not specified
Year:
Not applicable
Region / City:
Not applicable
Subject:
Research ethics and manuscript submission
Document Type:
Submission Template
Organization / Institution:
Not applicable
Author:
Not applicable
Target Audience:
Researchers, Authors submitting manuscripts
Period of validity:
Not applicable
Approval Date:
Not applicable
Date of Changes:
Not applicable
Note:
Year
Region / City:
Buffalo, NY
Topic:
Research Study Consent
Document Type:
Informed Consent Form
Institution:
University at Buffalo
Author:
University at Buffalo Research Compliance
Target Audience:
Research Participants
Year:
2016
Region / City:
United States
Topic:
Electronic Informed Consent (eIC)
Document Type:
Guidance
Agency / Institution:
Office for Human Research Protection (OHRP), Food and Drug Administration (FDA)
Author:
Office for Human Research Protection (OHRP), FDA
Target Audience:
Researchers, IRBs, Clinical Investigators, and Study Participants
Period of Validity:
Ongoing
Approval Date:
December 2016
Date of Revisions:
Not specified
Year:
2018
Region / City:
United States
Theme:
Cancer prevention, clinical trials
Document Type:
Template
Organ / Institution:
National Cancer Institute (NCI), National Institutes of Health (NIH)
Author:
NCI
Target Audience:
Researchers, clinical trial participants
Period of Validity:
Ongoing
Approval Date:
January 19, 2018
Date of Changes:
N/A
Note:
Year
Topic:
Human Subject Research
Document Type:
Informed Consent Form
Organization / institution:
Coastal Carolina University
Author:
[PI Name]
Target Audience:
Potential research participants