№ lp_1_2_32914
File format: docx
Character count: 43493
File size: 124 KB
This document provides guidance on creating the Organisation Information Document for submitting with the IRAS Form, primarily aimed at participating NHS / HSC organizations in the UK.
Year:
2023
Region / City:
United Kingdom
Topic:
Clinical Research
Document Type:
Template
Organization/Institution:
The University of Nottingham
Author:
Not specified
Target Audience:
NHS / HSC organizations, Sponsors, CROs
Period of Activity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
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Year:
2023
Region / City:
United Kingdom
Topic:
Clinical Trials, Healthcare
Document Type:
Template
Organization / Institution:
University Hospitals Bristol and Weston NHS Foundation Trust
Author:
Not specified
Target Audience:
Researchers, Sponsors, NHS / HSC Organizations
Period of validity:
Until the completion of the study
Approval Date:
Not specified
Amendment Date:
Not specified
Note:
Year
Subject:
Data Protection, GDPR Compliance
Document Type:
Agreement, Data Processing Agreement
Target Audience:
Participating NHS / HSC Organisations, Sponsors
Contextual description:
Data processing agreement for non-commercial research studies between Sponsor and Participating NHS / HSC Organisation.
Year:
2024
Note:
Region / City
Theme:
Research Study Setup
Document Type:
Template
Target Audience:
Sponsor/Co-Sponsors, Participating NHS/HSC Organisations
Note:
Year
Year:
2024
Region / city:
UK
Topic:
Data Processing Agreement
Document type:
Template
Organisation:
NHS / HSC Organisation
Author:
N/A
Target audience:
Academic institutions, healthcare organisations
Period of validity:
N/A
Approval date:
N/A
Date of changes:
March 2024
Year:
2023
Region / City:
United Kingdom
Topic:
Clinical Trials, Healthcare
Document Type:
Template
Organization / Institution:
University Hospitals Bristol and Weston NHS Foundation Trust
Author:
Not specified
Target Audience:
Researchers, Sponsors, NHS / HSC Organizations
Period of validity:
Until the completion of the study
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
20__
Note:
Region/City
Document Type:
Project Study Report
Year:
2026
Region / City:
London
Subject:
Clinical Research Protocol
Document Type:
Template
Institution:
University College London Hospitals NHS Foundation Trust (UCLH)
Author:
UCLH Research Office
Target Audience:
UCLH Investigators, Clinical Researchers
Study Duration:
Ongoing
Approval Date:
Not specified
Date of Modification:
Not specified
Note:
Year
Note:
Year
Subject:
Data Protection, GDPR Compliance
Document Type:
Agreement, Data Processing Agreement
Target Audience:
Participating NHS / HSC Organisations, Sponsors
Contextual description:
Data processing agreement for non-commercial research studies between Sponsor and Participating NHS / HSC Organisation.
Year:
2024
Note:
Region / City
Theme:
Research Study Setup
Document Type:
Template
Target Audience:
Sponsor/Co-Sponsors, Participating NHS/HSC Organisations
Note:
Year
Note:
Year
Document Type:
Template and Guidelines
Sponsoring Institution:
National Institute on Aging (NIA)
Intended Use:
Clinical study planning
Target Audience:
Investigators conducting clinical trials
Content Focus:
Data and safety monitoring, adverse event reporting, interim analysis, participant protection
Study Phase:
Applicable to all behavioral and intervention studies
Sections Included:
Participant safety, interim analysis, data and safety monitoring, DSMB responsibilities, confidentiality protection
Year:
2016
Region / City:
Stafford, VA
Topic:
Science Education, Special Needs
Document Type:
Registration Form
Institution:
VSDB (Virginia School for the Deaf and the Blind)
Author:
Dr. Debbie Pfeiffer
Target Audience:
Families of students with hearing disabilities
Event Date:
Oct. 8, 2016
Date of Approval:
Not specified
Date of Changes:
Not specified
Year:
2016–
Country:
United States
Subject:
Compensation claims for victims of state sponsored terrorism
Document type:
Application instructions
Program:
U.S. Victims of State Sponsored Terrorism Fund
Administering authority:
U.S. Department of Justice
Legal basis:
Justice for United States Victims of State Sponsored Terrorism Act
Submission method:
Online claims portal
Language requirement:
English
Eligibility basis:
Final court judgment
Filing deadline rule:
90 days after final judgment
Privacy framework:
Privacy Act of 1974
Contact information included:
Yes
Year:
2024
Region / City:
Morgantown, West Virginia
Topic:
Occupational Safety and Health, Spirometry Training
Document Type:
Federal Regulation and Approval Request
Institution:
National Institute for Occupational Safety and Health
Author:
Kathleen Rogers, BS, RRT, CPFT
Target Audience:
Sponsors and applicants for NIOSH-approved spirometry training courses
Validity Period:
5 years (for course renewal)
Approval Date:
January 2, 2024
Date of Revisions:
None indicated
Note:
Year