№ lp_1_11778
File format: docx
Character count: 4749
File size: 43 KB
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
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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:
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
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:
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
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
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:
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
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