№ lp_1_2_43617
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This document provides local context language for the NCI CIRB model consent template, specifying how it should be used in research studies, including sections on signature lines, financial information, and institutional conflict of interest disclosures.
Year:
2018
Region / City:
Dana-Farber/Harvard Cancer Center
Topic:
Research Consent Forms
Document Type:
Institutional Consent Language
Organization / Institution:
Dana-Farber/Harvard Cancer Center (DF/HCC)
Author:
N/A
Target Audience:
Research participants and their legal representatives
Effective Period:
N/A
Approval Date:
10.04.2018
Date of Changes:
N/A
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Year:
2026
Region / City:
Boston, MA
Subject:
Clinical Trials, Consent Forms
Document Type:
Consent Form Template
Institution:
Dana-Farber/Harvard Cancer Center (DF/HCC)
Author:
DF/HCC Research Team
Target Audience:
Researchers, Study Coordinators, Institutional Review Boards
Effective Period:
Ongoing
Approval Date:
2026
Revision Date:
Not specified
Note:
Year
Year:
2023
Region / city:
N/A
Topic:
Clinical Trial Consent
Document Type:
Research Protocol
Organization / Institution:
DF/HCC
Author:
N/A
Target Audience:
Parents or Guardians of Children Participating in Clinical Trials
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
2023
Note:
Region / City
Topic:
Research Protocol
Document Type:
Template
Organization / Institution:
DF/HCC
Target Audience:
Investigators, Research Institutions
Note:
Year
Target Audience:
Research Personnel, Principal Investigator, Research Pharmacy Personnel
Year:
2026
Region / City:
Boston, MA
Subject:
Clinical Trials, Consent Forms
Document Type:
Consent Form Template
Institution:
Dana-Farber/Harvard Cancer Center (DF/HCC)
Author:
DF/HCC Research Team
Target Audience:
Researchers, Study Coordinators, Institutional Review Boards
Effective Period:
Ongoing
Approval Date:
2026
Revision Date:
Not specified
Year:
2020
Region / City:
United States
Subject:
NCI CIRB process for research protocol approval
Document Type:
Instructional Guide
Author:
NCI CIRB
Target Audience:
Investigators, research staff, and affiliated personnel
Period of Validity:
N/A
Approval Date:
2020
Date of Last Revision:
2020
Year:
2021
Region / City:
Wisconsin
Topic:
Informed Consent Form Template
Document Type:
Template
Organization / Institution:
Medical College of Wisconsin
Author:
NCI CIRB
Target Audience:
Researchers, Institutional Review Boards
Period of Validity:
Ongoing
Approval Date:
N/A
Modification Date:
N/A
Year:
2027
Region / City:
United States
Theme:
Clinical Research, Institutional Review Boards
Document Type:
Agreement
Organization / Institution:
National Cancer Institute (NCI)
Author:
National Cancer Institute (NCI)
Target Audience:
Institutions involved in clinical trials
Period of Action:
Ongoing until the expiration of agreement
Approval Date:
N/A
Date of Changes:
N/A
Year:
2019
Region / City:
United States
Topic:
Clinical Trials, Institutional Review Boards
Document Type:
Policy
Organization / Institution:
National Cancer Institute (NCI)
Author:
NCI
Target Audience:
NCTN and NCORP Sites, Clinical Trial Sites
Effective Period:
From March 1, 2019
Approval Date:
March 1, 2019
Modification Date:
Not specified
Year:
2023
Region / City:
United States
Subject:
Clinical Trial Studies, Institutional Review Board (IRB)
Document Type:
Authorization Agreement, Confidentiality Statement
Organization / Institution:
National Cancer Institute (NCI), CIRB
Author:
National Cancer Institute
Target Audience:
Institutions participating in clinical trials
Effective Period:
Until March 31, 2026
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2026
Region / City:
Boston, MA
Subject:
Clinical Trials, Consent Forms
Document Type:
Consent Form Template
Institution:
Dana-Farber/Harvard Cancer Center (DF/HCC)
Author:
DF/HCC Research Team
Target Audience:
Researchers, Study Coordinators, Institutional Review Boards
Effective Period:
Ongoing
Approval Date:
2026
Revision Date:
Not specified
Note:
Year
Subject Matter:
Research Ethics
Document Type:
Protocol
Institution:
Massachusetts Institute of Technology
Author:
Committee on the Use of Humans as Experimental Subjects
Target Audience:
Researchers and Institutions engaging in human subjects research
Contextual Description:
A protocol document for institutions requesting MIT to serve as the reviewing IRB in human subjects research.
Year:
No data
Region / City:
No data
Theme:
Christianity, Faith, Spirituality
Document Type:
Religious Text
Author:
No data
Target Audience:
Christians, Believers
Period of Action:
No data
Approval Date:
No data
Amendment Date:
No data
A sermon or religious reflection on finding joy in Christ, derived from the biblical passage John 16:
16-33.
Year:
2020
Region / City:
United States
Subject:
NCI CIRB process for research protocol approval
Document Type:
Instructional Guide
Author:
NCI CIRB
Target Audience:
Investigators, research staff, and affiliated personnel
Period of Validity:
N/A
Approval Date:
2020
Date of Last Revision:
2020
Document Type:
Institutional guidance document
Subject:
Reliance arrangement procedures and study team responsibilities
Related Agreement:
SMART IRB Master Common Reciprocal Institutional Review Board Authorization Agreement
Governing Procedures:
SMART IRB Standard Operating Procedures (SOPs)
Issuing Body:
Reviewing Institutional Review Board
Applicable To:
Relying Site Study Teams
Scope:
Multi-site research relying on a single IRB
Key Roles Identified:
Lead Study Team; SMART IRB Point of Contact (POC)
Topics Covered:
Communication plan; IRB approval preparation; reporting requirements; compliance obligations; key IRB policies
Referenced Materials:
Communication Plan; FAQs for Research Teams Relying on an External IRB
Regulatory Framework:
Applicable federal regulations; state and local laws; institutional requirements
Lifecycle Coverage:
Study activation, conduct, continuing review, reporting, and site closure
Institution:
Wayne State University
Department / Office:
Institutional Review Boards (IRBs)
IRB Panels:
PH1, MI, MP2 – Medical; B3 – Social, Behavioral, Education
Document Type:
Research administration form
Document Purpose:
Collection of institutional and regulatory information for reliance arrangements in human subjects research
Related Agreement:
SMART IRB Agreement (if applicable)
Regulatory Framework:
Human subjects research oversight
Related Regulation:
HIPAA (Protected Health Information)
Accreditation Reference:
AAHRPP
Research Context:
Multi-site research studies with relying institutions
Responsible Roles Mentioned:
WSU Principal Investigator (PI), Relying Institution PI, Institutional oversight personnel
Key Topics:
Institutional oversight, conflict of interest review, protocol compliance, participant protections, reporting of noncompliance, consent form language requirements, regulatory coordination
Geographic Scope:
United States and international relying institutions (when applicable)
Applicable Research Type:
Medical, social, behavioral, and educational research involving human subjects