№ lp_1_2_40950
File format: docx
Character count: 65982
File size: 184 KB
Structured survey form for hospitals to report trauma care capabilities, staff, patient statistics, and compliance with Level IV trauma facility standards for state evaluation.
Year:
2023
State:
Wisconsin
Type of Document:
Questionnaire / Data Collection Form
Institution:
Department of Health Services, Division of Public Health
Program:
Trauma Program
Target Audience:
Hospitals seeking Level IV trauma classification
Reporting Period:
12 months prior to PRQ submission
Submission Deadline:
45 days before scheduled site visit
Contact Email:
[email protected]
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.
The file will be delivered to the email address provided at checkout within 12 hours.
Don’t have cryptocurrency yet?
You can still complete your purchase in a few minutes:- Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
- In the app, tap Send.
- Select network, paste our wallet address.
- Send the exact amount shown above.
The final amount may vary slightly depending on the payment method.
The file will be sent to the email address provided at checkout within 24 hours.
The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2023
Region / City:
United States
Topic:
Citizen Science, Crowdsourcing, Public Health Research
Document Type:
Official Agency Statement
Organization:
National Institutes of Health (NIH)
Author:
Mikia Currie, Chief, Project Clearance Branch
Target Audience:
Researchers, Program Staff, Federal Agencies, Public Participants
Effective Period:
July 26, 2023
Approval Date:
July 26, 2023
Amendment Date:
Not specified
Year:
2023
Location:
London, UK / Beirut, Lebanon
Document Type:
Tender / Price Quotation Form
Organization:
Consulate General of Brazil in London
Addressee:
Mr. Luiz Roberto Avelino Reciolino
Services Covered:
Relocation, Freight, Insurance, Storage, Taxes, Handling Charges
Currency:
As specified in the form
Validity Period:
Prices valid until specified date
Submission Requirement:
Complete all fields, N/A or Free of Charge if not applicable
Document Category:
Official tender document for relocation services
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.
Note:
Year
Topic:
Procurement, Equipment, Services, Software
Document Type:
Checklist
Organization:
County APD
Note:
Year
HRP-308 Worksheet: Pre-Review Screening Checklist for Human Research Submissions (February 16, 2026)
Year:
2026
Date:
February 16, 2026
Document Code:
HRP-308
Document Type:
Worksheet
Subject:
Human Research Ethics Review and IRB Pre-Review Screening
Responsible Body:
Institutional Review Board (IRB)
Purpose:
Screening of submission materials for Human Research review
Related Documents:
HRP-309 Ancillary Review Matrix; HRP-330 HIPAA Authorization Worksheet; HRP-024 SOP New Information; HRP-306 Drugs Worksheet; HRP-307 Devices Worksheet; HRP-801 Establishing Reliance Agreements; HRP-815 Institutional Profile Form; HRP-830 Communication and Responsibilities Worksheet
Regulatory Areas Referenced:
Human Research Regulations; EU GDPR; HIPAA; NIH Policy; FERPA; PPRA
Primary Users:
IRB staff conducting submission screening
Scope:
Initial review, modification review, and pSite review for studies relying on the IRB
Key Topics:
regulatory oversight determination, ancillary reviews, ethics training verification, conflict of interest disclosure, consent documentation, research protocol completeness, drug and device oversight, multi-site research coordination, HIPAA authorization review, protection of vulnerable populations
Note:
Year
Context:
This document outlines the process for Clinical Faculty to complete a Pre-Review of Payroll Statements in the PAC system for certification.
Year:
Not specified
Region:
Oregon
Document type:
Guidelines
Survey type:
Virtual trauma hospital survey
Trauma center levels:
Levels I–IV
Issuing body:
Oregon Health Authority
Program:
EMS & Trauma Systems
Intended participants:
Trauma hospitals and trauma program staff
Survey format:
Virtual
Technology platform:
Zoom for Government
Pre-survey submission timeline:
Two months prior to scheduled survey
Medical record submission deadline:
At least one week prior to scheduled survey
Survey components:
Pre-survey review, medical chart review, interviews, exit interview
Patient data scope:
Trauma census, outcomes, injuries, transfers, readmissions, deaths
Governing authority contacts:
Oregon Health Authority EMS Program
Note:
Year
Theme:
Trauma Care, Health Services
Document Type:
Application
Organization / Institution:
Kentucky Cabinet for Health and Family Services
Author:
Kentucky Trauma Advisory Committee
Target Audience:
Healthcare Facilities, Trauma Centers
Year:
2024
Region / City:
Ireland
Topic:
Healthcare, Rehabilitation, Trauma
Document Type:
Rehabilitation Guideline
Organization:
Health Service Executive (HSE)
Author:
National Office for Trauma Services
Target Audience:
Healthcare professionals in the trauma care system
Period of validity:
September 2024 - September 2025
Approval Date:
September 2024
Revision Date:
September 2025
Responsibility for Review and Audit:
Trauma System Implementation Programme
Year:
2026
Organization:
Canberra Health Services (CHS)
Document Type:
Procedure
Scope:
CHS medical, nursing, allied health, radiography, and ward staff involved in trauma care
Target Audience:
Trauma Team members, ED staff, ICU staff, surgical registrars
Attachments:
ACT Trauma Service (ACTTS) Trauma ‘CODE’ Guideline Triage Cat 1; ACTTS Trauma ‘ALERT’ Guideline Triage Cat 2
Related Policies:
Emergency Department triage protocols, Australian Triage Scale (ATS)
Purpose:
Outline immediate assessment, resuscitation, and management of life-threatening injuries
Sections:
Trauma Team, Trauma Code, Trauma Alert, Alert Upgrade, Minor Trauma Review, Trauma Team conduct and organisation, Evaluation, References, Definition of Terms
Year:
2021
Region / City:
Australia
Topic:
Road Safety, Vehicle Standards, Autonomous Emergency Braking (AEB)
Document Type:
Regulation Impact Statement
Organization / Institution:
Department of Infrastructure, Transport, Regional Development and Communications
Author:
Department of Infrastructure, Transport, Regional Development and Communications
Target Audience:
Policymakers, Vehicle Manufacturers, Road Safety Experts
Action Period:
July 2021 and beyond
Approval Date:
July 2021
Date of Changes:
N/A
Year:
2014
Region / City:
United States
Subject:
Trauma Center Designation Criteria
Document Type:
Guidelines
Institution:
American College of Surgeons
Author:
American College of Surgeons
Target Audience:
Healthcare professionals involved in trauma care
Period of validity:
Indefinite
Approval Date:
2014
Date of amendments:
N/A
Year:
2025
Region / City:
Massachusetts
Subject:
Trauma Registry Data Submission
Document Type:
Regulatory Guide
Institution:
Massachusetts Department of Public Health, Bureau of Health Care Safety and Quality
Author:
Massachusetts Department of Public Health
Target Audience:
Healthcare Facilities, Trauma Centers, Hospitals
Period of Application:
January 1, 2025 – December 31, 2025
Approval Date:
N/A
Date of Changes:
N/A
Note:
Year
Organization / Institution:
Emergency Medicine Foundation
Year:
2008
Region / city:
USA
Theme:
Trauma Care
Document Type:
Clinical Guideline
Organization / Institution:
American College of Surgeons
Author:
American College of Surgeons Committee on Trauma
Target Audience:
Healthcare professionals in trauma care
Period of validity:
Indefinite
Approval Date:
2008
Date of Changes:
Not specified
Contextual Description:
Clinical guideline defining the procedure and components of a tertiary survey in trauma care to reduce missed injuries after initial treatment and operative intervention.
Year:
2026
Region / city:
Australia
Topic:
Aged care, trauma-informed care
Document type:
Briefing note
Organization / institution:
Helping Hand Aged Care
Author:
Not specified
Target audience:
Executive Leadership Team, Board
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Year:
2023
Region / City:
Massachusetts
Topic:
Trauma Registry, Data Submission
Document Type:
Regulatory Submission Guide
Organization / Institution:
Massachusetts Department of Public Health, Bureau of Health Care Safety and Quality
Author:
Massachusetts Department of Public Health
Target Audience:
Hospitals, Health Care Providers, Data Submitters
Period of Action:
January 1, 2023 - December 31, 2023
Approval Date:
January 1, 2023
Change Date:
No specified change date