№ lp_1_29083
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Character count: 25996
File size: 387 KB
A guideline providing rugby clubs and schools in New Zealand with detailed COVID-19 safety protocols for match day activities under the government’s COVID-19 Protection Framework.
Year:
2022
Region / city:
New Zealand
Topic:
Rugby, COVID-19 Guidelines
Document Type:
Guideline
Organization:
New Zealand Rugby
Author:
New Zealand Rugby
Target Audience:
Rugby clubs, schools, participants, coaches, and managers
Period of Action:
Ongoing, subject to updates based on COVID-19 Protection Framework
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Contextual Description
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2025
Region / city:
United Kingdom
Subject:
Sports broadcasting, Rugby League, Super League, Challenge Cup
Document type:
Invitation to Tender (ITT)
Organization / institution:
BBC
Author:
BBC Sport
Target audience:
Production companies, tenderers
Period of validity:
2026
Approval date:
22nd September 2025
Date of amendments:
N/A
Year:
2025
Region / city:
New Zealand
Topic:
Rugby, Medical Certification
Document Type:
Approval Form
Organization / Institution:
New Zealand Rugby (NZR)
Author:
Not specified
Target Audience:
Players, Parents, Legal Guardians, Medical Professionals
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Note:
Year
Theme:
Risk Management
Document Type:
Risk Assessment
Year:
2014
Region / City:
Minnesota
Theme:
Youth Rugby, Sports Development
Document Type:
Meeting Minutes
Organization:
Minnesota Youth Rugby
Author:
Rob Clarno
Target Audience:
MYR Board, MYR Members
Date of Approval:
8/26/2014
Date of Changes:
N/A
Year:
2023
Region / City:
Global
Topic:
Harassment prevention in sports
Document type:
Policy
Organization / Institution:
International Wheelchair Rugby Federation
Author:
International Wheelchair Rugby Federation
Target audience:
Athletes, coaches, volunteers, staff, technical officials, and IWRF members
Period of validity:
Ongoing
Approval date:
Not specified
Date of amendments:
Not specified
Context:
A policy document outlining the stance and measures against harassment within the International Wheelchair Rugby Federation, including various forms of harassment and the procedures for addressing them.
Note:
Year
Subject:
Statistics
Document type:
Educational material
Target audience:
Students, educators
Year:
2021
Region / City:
Cornwall
Topic:
Rugby, Sports Trials
Document Type:
Nomination Form
Organization:
Cornwall County Rugby
Author:
Melissa Rowe
Target Audience:
Coaches, Parents, Players
Period of Action:
January – February 2021
Approval Date:
N/A
Date of Changes:
N/A
Organisation:
Devon Rugby Referee Society (DRRS)
Associated Body:
Rugby Football Union (RFU)
Document Type:
Code of Conduct
Subject:
Core Values and Standards of Behaviour
Core Values:
Integrity, Honesty, Credibility, Impartiality
Applicability:
Members and Officials of DRRS
Scope:
Officiating Duties and Representation of the Society
Obligations:
Professional Conduct, Media Authorisation, Confidentiality, Impartial Decision-Making
Prohibitions:
Misuse of Position, Acceptance of Compromising Benefits, Unauthorised Disclosure, Bias
Purpose:
Definition of expected standards of behaviour in officiating and representation
Organisation:
BokSmart
Website:
https://my.boksmart.com
Associated Organisation:
South African Rugby Union (SARU)
International Governing Body:
World Rugby (formerly International Rugby Board)
Related Fund:
Chris Burger/Petro Jackson Players Fund
Document Type:
Injury report form
Subject:
Reporting of serious and/or catastrophic rugby injuries
Geographical Scope:
South Africa
Target Group:
Rugby players, parents, guardians, schools, clubs, teams, provincial unions
Data Processing:
Collection, storage and research use of injury data
Consent Requirement:
Player and/or parent/guardian/family member consent
Submission Deadline:
Within 48 hours of injury
Submission Method:
Fax or email to Serious Injury Case Manager
Responsible Officer:
Serious Injury Case Manager (SICM)
Database:
SARU catastrophic injury database and World Rugby secure database
Confidentiality:
Personal information treated as confidential in research analyses
Provincial Contacts:
Listed BokSmart Coordinators of provincial unions in South Africa
Year:
2024
Region / City:
Not specified
Topic:
Risk Assessment
Document Type:
Safety Protocol
Organization:
LSSP
Author:
Dani McGifford
Target Audience:
Staff, Participants, Volunteers
Period of Validity:
2024
Date Approved:
17/06/2024
Date of Amendments:
Not specified
Year:
2025
Competition:
Horsley Zone Winter PSSA
Sport:
Rugby League
Divisions:
Junior; Senior
Round Covered:
After Round 9
Last Updated:
29.8.25
Region:
Horsley Zone
Participating Teams (Junior):
GPK; FW; KP; WS; HS; Chi; Smi; SJP
Participating Teams (Senior):
FW; GPK; Smi; CW; Che; Chi; HS; WS
Document Type:
Competition ladder and match results table
Season Period:
May–August 2025
Year:
2026
Region / City:
UK
Topic:
Sports Education, Teaching Role
Document Type:
Job Specification
Institution:
Myerscough College and University Centre
Author:
Myerscough College
Target Audience:
Applicants for Practical Skills Tutor role in Rugby Coaching and Strength & Conditioning
Period of Activity:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
Not provided
Region / City:
Not specified
Topic:
Research ethics, manuscript submission
Document type:
Template
Author:
Not specified
Target audience:
Authors submitting research articles
Period of validity:
Not provided
Approval date:
Not specified
Date of changes:
Not specified
Investigator:
[insert name of principal investigator]
Key Information:
The following is a short summary of this study to help you decide whether or not to be a part of this study. More detailed information is listed later on in this form.
Note:
Why am I being invited to take part in a research study?
You will be asked to _________ [include a high level summary of the procedures that will be done. For example:
You will be given an investigational drug and asked to come for 3 study visits. You will give a total of 3 blood samples and fill out questionnaires asking about how you feel.]
Instead of being in this research study, your choices may include:
[List alternatives procedures. For student subject pools describe alternatives for course credit. For clinical trials describe the options that you would normally offer patient. If applicable, include supportive care as an option.]
Detailed Information:
The following is more detailed information about this study in addition to the information listed above.
[Tell the subject what to expect using lay language and simple terms. Whenever appropriate include the following items:
]
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:
2025
Region / City:
Hills
Theme:
Bowls competition regulations
Document Type:
Rules
Organization:
Hills Bowling Association
Author:
Hills Bowling Association Executive Committee
Target Audience:
Affiliated Clubs, Players, Officials
Period of Validity:
Ongoing
Approval Date:
6.1.25
Date of Amendments:
6.1.25
Year:
2022
Region / City:
United States
Topic:
Education, Financial Flexibility
Document Type:
Official Letter
Organization / Institution:
United States Department of Education, Office of Postsecondary Education
Author:
Michelle Asha Cooper, Ph.D.
Target Audience:
GEAR UP Grantee Project Directors
Effective Period:
From March 13, 2020, to September 30, 2023
Approval Date:
July 27, 2022
Amendment Date:
None