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This document is a submission form for educational institutions to request accreditation of engineering programmes by the Engineering Council.
Year:
2023
Region / City:
UK
Theme:
Accreditation
Document Type:
Submission Form
Organization:
Engineering Council
Author:
Leila Atherton
Target Audience:
Educational Institutions, Staff
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
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Year:
2023
Region / city:
UK
Topic:
Technical report for Stage 1 submission
Document type:
Accreditation document
Organization:
CIHT (Chartered Institution of Highways and Transportation)
Author:
CIHT
Target audience:
Engineers seeking accreditation
Period of validity:
N/A
Approval date:
N/A
Date of revisions:
N/A
Year:
2025
Region / city:
Wisconsin
Subject:
Transportation, Environmental Coordination
Document Type:
Request Form
Organization / institution:
Wisconsin Department of Transportation (WisDOT)
Author:
Wisconsin Department of Transportation (WisDOT)
Target Audience:
WisDOT staff, Environmental Coordinators
Period of validity:
Not specified
Approval Date:
Not specified
Date of changes:
Not specified
Year:
2020
Region / city:
Bangladesh
Theme:
Rights of persons with disabilities
Document type:
Report
Organization / institution:
United Nations
Author:
Committee on the Rights of Persons with Disabilities
Target audience:
Government bodies, policymakers, stakeholders in the disability sector
Period of validity:
2019–2025
Approval date:
23 December 2019
Date of amendments:
Not specified
Note:
Year
Topic:
Incident Investigation
Document Type:
Report
Target Audience:
Management, HR, Investigation Team
Year:
2027
Region / city:
United States
Topic:
Medicare Drug Price Negotiation Program
Document type:
Supporting Statement
Organ / institution:
Centers for Medicare & Medicaid Services (CMS)
Author:
Centers for Medicare & Medicaid Services (CMS)
Target audience:
Pharmaceutical industry, healthcare professionals, policymakers
Period of validity:
2026-2028
Approval date:
Not specified
Modification date:
Not specified
Year:
2021
Region / city:
United States
Subject:
Patent applications and legal requirements
Document type:
Official form
Organization / institution:
United States Patent and Trademark Office
Author:
United States Patent and Trademark Office
Target audience:
Patent applicants, legal professionals
Validity period:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Year:
2023
Location:
Atlanta, GA, USA
Document Type:
Working Instructions / Inventory Form
Regulatory Authority:
Drug Enforcement Administration (DEA)
Author:
Joe Smith
Intended Audience:
DEA Registrants and laboratory staff
Inventory Scope:
Schedule I – II and Schedule III – V Controlled Substances
Inventory Date:
05/01/23
Inventory Time:
Beginning of Business (BOB) / Close of Business (COB)
Employees Conducting Inventory:
Joe Smith, Joann Taylor
Year:
2025-2026
Region / City:
UK
Theme:
Teacher Education
Document Type:
Partnership Agreement
Institution:
Edge Hill University
Author:
Not specified
Target Audience:
Schools, Colleges, Teacher Trainees
Period of Validity:
2025-2026
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2007
Region / city:
South Africa
Topic:
Certification
Document type:
Guideline
Institution:
South African Qualification and Certification Committee for Inspectors of Pressurised Equipment
Author:
SAQCC-IPE
Target audience:
Applicants for IPE certification
Validity period:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Note:
Year
Document Type:
Template Assessment Form
Organization / Institution:
North East and North Cumbria Provider Collaborative, British Dietetic Association (BDA)
Target Audience:
Clinicians, Mental Health Professionals, Carers
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.
Year:
2023
Region / City:
Central Florida
Subject:
Procurement Evaluation Process
Document Type:
Procedural Guidelines
Organization / Institution:
Central Florida Behavioral Health Network, Inc. (CFBHN)
Author:
Carrie Hartes, Procurement Manager
Target Audience:
Evaluation Team Members, Procurement Personnel
Period of Action:
Ongoing
Approval Date:
N/A
Date of Modifications:
N/A
Year:
2025
Region/City:
California
Subject:
Environmental Documentation
Document Type:
Template
Agency/Institution:
Caltrans
Author:
Not specified
Target Audience:
Government Agencies, Environmental Consultants
Effective Period:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2024
Region / City:
New York
Topic:
Research submission process
Document type:
Checklist
Organization / Institution:
Mount Sinai Health System
Author:
Not specified
Target audience:
Research teams at Mount Sinai
Period of validity:
Indefinite
Approval date:
Not specified
Modification date:
Not specified
Contextual description:
A procedural checklist for research teams preparing initial study submissions through the RUTH system at Mount Sinai Health System.
Year:
2026
Region / City:
United States
Topic:
Federal procurement and contract management
Document Type:
Policy/Guidance
Agency / Institution:
GSA (General Services Administration)
Author:
GSA
Target Audience:
Contractors, Government Agencies
Period of Validity:
Ongoing
Approval Date:
N/A
Modification Date:
N/A
Year:
Not specified
Region / City:
Not specified
Topic:
Corporate Experience, Relevant Project Experience
Document Type:
Solicitation Guidelines
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Contractors, Offerors
Period of Validity:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Note:
Year
Topic:
KiwiSaver, default provider, investment mandate, responsible investment
Document type:
Submission template