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This document is an organisational template for submitting study information to the IRAS system, specifically for non-commercial studies, outlining local requirements and responsibilities for participating NHS/HSC organisations.
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Organisation Information Document (Data Processing Agreement ONLY) – Non-commercially sponsored projects(Template version: 1.1)
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.
Organisation Information Document – Non-Commercially Sponsored Studies (Template version: 1.8 April 2024)
Year: 2024
Note: Region / City
Theme: Research Study Setup
Document Type: Template
Target Audience: Sponsor/Co-Sponsors, Participating NHS/HSC Organisations
Organisation Information Document – Non-Commercially Sponsored Studies (Template version: 1.6)
Note: Year
Organisation Information Document – Non-Commercially Sponsored Studies(Template version: 1.6)
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
Organisation Information Document (Data Processing Agreement ONLY) – Non-commercially sponsored projects(Template version: 1.2 March 2024)
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
Organisation Information Document – Non-Commercially Sponsored Studies(Template version: 1.6)
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
Project Study Report-Project Development Support (PSR-PDS)ToRequest Programming for Capital Support(Project Approval and Environmental Document Phase) (in the 20__ STIP)*(*For a locally sponsored project, this language may not be included or may need to be modified.)
Year: 20__
Note: Region/City
Document Type: Project Study Report
Observational Protocol Template for UCLH/UCL Sponsored Studies
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
Externally Sponsored Research Fee Template
Note: Year
Organisation Information Document (Data Processing Agreement ONLY) – Non-commercially sponsored projects(Template version: 1.1)
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.
Organisation Information Document – Non-Commercially Sponsored Studies (Template version: 1.8 April 2024)
Year: 2024
Note: Region / City
Theme: Research Study Setup
Document Type: Template
Target Audience: Sponsor/Co-Sponsors, Participating NHS/HSC Organisations
Organisation Information Document – Non-Commercially Sponsored Studies (Template version: 1.6)
Note: Year
DATA & SAFETY MONITORING PLAN (DSMP) Template and Guidelines for Clinical Studies Sponsored by NIA
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
Registration Form for “Science with Jefferson Lab” Sponsored by Outreach Services, VSDB in Collaboration with Stafford Co. Public Schools & Jefferson Lab Saturday, Oct. 8, 2016, 9:30 am – 2:30 pm
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
Serious Adverse Event - report form B (For all UoL sponsored studies excluding clinical trials of investigational medicinal products)
Note: Year
Application Form Instructions for Claims to the U.S. Victims of State Sponsored Terrorism Fund
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
PULMONARY FUNCTION TESTING COURSE APPROVAL PROGRAM Regulation 29 CFR 1910.1043 (h) (1) (iii)(0920-0138) Request for Office of Management and Budget (OMB) Review and Approval for a Federally Sponsored Data Collection Revision
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
THIS SPONSORED RESEARCH AGREEMENT
Note: Year
Sponsored Researcher Certificate of Sponsorship (CoS) Application Form– Guidance Notes
Note: Year
Organisation Information Document – Non-Commercially Sponsored Studies(Template version: 1.6)
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
Topics: Non-commercially sponsored Organisation