№ lp_2_3_45691
File format: docx
Character count: 19779
File size: 650 KB
This is an informed consent document for a clinical research study, detailing the nature of participation, risks, and procedures involved.
Year:
2023
Region / city:
United States
Subject:
Clinical research, informed consent
Document type:
Informed Consent Form
Institution:
MedStar Health Research Institute
Author:
Not specified
Target audience:
Research participants
Period of validity:
Not specified
Approval date:
Not specified
Modification date:
Not specified
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Organization:
MedStar Health
Document Type:
Patient Information Sheet
Policy Name:
MedStar Health Financial Assistance Policy (FAP)
Geographic Scope:
Maryland and Washington, DC
Subject:
Financial Assistance for Emergency and Medically Necessary Hospital Services
Eligibility Criteria:
Households below 200% of the Federal Poverty Level for free care; up to 400% for reduced-cost care
Related Programs:
Maryland Medicaid; DC Medical Assistance
Contact Phone Numbers:
(410) 933-4966; (844) 817-6087
Mailing Address for Applications and Appeals:
PO Box 411019, Boston, MA 02241-1019
Appeal Period:
Within ten days of receipt of determination
Website:
www.medstarhealth.org/FinancialAssistance
Issuing Entity:
MedStar Health Hospitals
Year:
2023
Region / City:
Metropolitan Area
Theme:
Emergency Medical Services, Public Safety, Healthcare Technology
Document Type:
Biography
Organization:
Metropolitan Area EMS Authority (MedStar Mobile Healthcare)
Author:
Frank Gresh
Target Audience:
Professionals in Emergency Medical Services, Healthcare, Public Safety
Date of Approval:
N/A
Date of Changes:
N/A
Context:
Biography of Frank Gresh, detailing his career in Emergency Medical Services, leadership roles, and contributions to technology in public safety.
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
Year:
Not specified
Region / City:
Not specified
Topic:
Research ethics, informed consent
Document Type:
Addendum
Institution / Organization:
Columbia University
Author:
Not specified
Target Audience:
Research participants
Period of validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Topic:
Research Ethics
Document Type:
Guidelines
Organization / Institution:
EIU IRB
Target Audience:
Researchers, Institutional Review Board Members
Year:
2025
Topic:
Free, Prior and Informed Consent (FPIC)
Document type:
Protocol
Organization / institution:
Blue Action Fund
Author:
Blue Action Fund
Target audience:
NGOs, project developers, indigenous peoples, local communities
Period of validity:
Not specified
Approval date:
Not specified
Date of modifications:
Not specified
Year:
2023
Region / City:
United States
Topic:
Informed Consent, Research Ethics
Document Type:
Research Guidelines
Organization:
U.S. Department of Health and Human Services, Office for Human Research Protections
Author:
Not specified
Target Audience:
Researchers, Institutional Review Board (IRB) members
Validity Period:
Not specified
Approval Date:
Not specified
Date of Last Update:
Not specified
Year:
2016
Region / City:
Dublin
Topic:
Research Consent Forms
Document Type:
Template
Organization:
Trinity College Dublin
Author:
Trinity College Dublin
Target Audience:
Researchers in historical, social, economic or scientific fields
Period of Validity:
Indefinite
Approval Date:
2016
Modification Date:
N/A
Context:
Template for preparing an informed consent form for use in historical, social, economic, or scientific research, ensuring compliance with EU General Data Protection Regulation.
Document type:
Instructional guidance
Subject:
Informed consent forms in clinical research
Context:
Clinical trials involving human participants
Regulatory and ethical framework:
Research ethics and regulatory compliance
Organizations referenced:
Children’s Oncology Group; National Cancer Institute; National Institutes of Health; OCREB
Funding context:
Public funding by the National Cancer Institute
Intended audience:
Consent form authors; clinical trial investigators; participating centres
Geographic scope:
North America
Population referenced:
Children and adolescents with cancer; parents or legal guardians
Related materials:
Provincial informed consent form templates; lay terminology glossary
Note:
Year
Document Type:
Research Consent Form
Organ / Institution:
Ross University School of Veterinary Medicine
Target Audience:
Animal owners
Year:
2026
Region / City:
Florida, USA
Subject:
Concussion awareness and head injury prevention
Document Type:
Informed consent form
Organization:
Davie Youth Lacrosse Foundation
Target Audience:
Parents/guardians and youth players
Purpose:
Acknowledgement of receipt of concussion information
Legal Requirement:
State of Florida mandatory concussion awareness
Note:
Year
Subject:
Emergency Use Treatment
Document Type:
Informed Consent Form
Note:
Year
Document type:
Checklist
Organization / Institution:
ACT Teacher Quality Institute
Target audience:
Experienced teachers applying for full registration
Year:
2024
Region / City:
South Carolina
Subject:
Transportation Services
Document Type:
Invitation for Bid
Organization / Institution:
South Carolina Department of Transportation
Author:
South Carolina Department of Transportation
Target Audience:
Vendors and Contractors
Effective Period:
December 2024 – January 2025
Approval Date:
11/14/2024
Amendment Date:
01/15/2025
Year:
2024
Region / City:
Hilton Head, SC
Theme:
Deafness, Accessibility, Professional Development
Document Type:
Call for Proposals
Organization:
Southeast Regional Institute on Deafness (SERID)
Author:
Not specified
Target Audience:
Professionals working with individuals who are deaf, deaf-blind, hard of hearing, and late-deafened
Period of Validity:
November 17-20, 2024
Approval Date:
Not specified
Date of Changes:
Not specified