№ lp_1_19422
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This document is an informed consent form used by ophthalmologists to explain the risks, benefits, and alternatives of Eylea treatment for patients with eye conditions such as macular edema and diabetic retinopathy.
Year: 2020
Region / City: N/A
Theme: Informed consent, medical treatment
Document type: Informed consent form
Organization / Institution: N/A
Author: N/A
Target Audience: Patients undergoing Eylea treatment, ophthalmologists
Effective period: N/A
Approval date: N/A
Amendment date: N/A
Price: 8 / 10 USD
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Summary of Product Characteristics for Eylea
Note: Year
Aflibercept Authority Required Listing Request for Subfoveal mCNV Treatment
Note: Year
Acknowledgment, Research Ethics, Informed Consent, Author Contributions, Use of Large Language Models, AI and Machine Learning Tools, Conflict of Interest, Research Funding, Data Availability
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
University at Buffalo Institutional Review Board (UBIRB) Informed Consent Form
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
Appendix I: Revised Guidance on Electronic Informed Consent (eIC) Released by OHRP and FDA in December 2016
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
INFORMED CONSENT FORM TEMPLATE
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
INFORMED CONSENT FOR HUMANSUBJECT RESEARCH PARTICIPATION
Note: Year
Topic: Human Subject Research
Document Type: Informed Consent Form
Organization / institution: Coastal Carolina University
Author: [PI Name]
Target Audience: Potential research participants
Checklist: Basic elements of the informed consent document
Note: Year
Addendum to the Informed Consent Document
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
Informed Consent Guidelines
Note: Year
Topic: Research Ethics
Document Type: Guidelines
Organization / Institution: EIU IRB
Target Audience: Researchers, Institutional Review Board Members
Free, Prior and Informed Consent (FPIC) Protocol
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
What is Informed Consent and Why is it Important?
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
GUIDANCE ON PREPARING AN INFORMED CONSENT FORM FOR HISTORICAL, SOCIAL, ECONOMIC OR SCIENTIFIC RESEARCH
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.
Instructions for Informed Consent Form Development for Clinical Trials
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
Guidance for PIs: Informed Consent for Animal Research Participation
Note: Year
Document Type: Research Consent Form
Organ / Institution: Ross University School of Veterinary Medicine
Target Audience: Animal owners
Concussion and Head Injury Informed Consent for Davie Youth Lacrosse Registration
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
Informed Consent for Emergency Use/Treatment with an Unapproved Drug / Biologic / Device 16.315 (HRP-506)
Note: Year
Subject: Emergency Use Treatment
Document Type: Informed Consent Form
Topics: Eylea aflibercept Informed