№ files_lp_3_process_7_043974
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Administrative compliance checklist documenting club confirmation of Covid-19 protocols and data protection measures for the organisation of an adult friendly football match under FAW regulations.
Document Type:
Checklist Form
Subject:
Return to Play Protocol Compliance
Related Protocol:
FAW Return to Play Protocol
Applicable To:
Adult Friendly Matches
Issuing Body:
Football Association of Wales (FAW)
Health Focus:
Covid-19
Requirements:
Covid-19 Compliance Officer Appointment
Note:
Requirements
Covid-19 Risk Assessment
Data Protection Reference:
GDPR
Retention Period:
28 Days (Participant Data)
Form Fields:
Proposed Fixture Details, Club Confirmation Responses, Signatory Details
Completion By:
Home or Away Club Representative
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2025–2026
Theme:
Baby Friendly Initiative standards and re-assessment
Document type:
Guidance notes
Programme:
UNICEF UK Baby Friendly Initiative
Assessment type:
Community re-assessment
Applicable period:
June 2025 – May 2026
Related standards:
Revised Baby Friendly standards
Assessment methods:
Interviews, document review, observations, internal audit validation
Target services:
Baby Friendly accredited community services
Audit tools referenced:
2019 audit tools; 2024 audit tool
Issuing body:
UNICEF UK Baby Friendly Initiative
Requirements status:
Required and recommended evidence specified
Transition phase:
Transition to revised standards
Year:
2023
Region / City:
Local Pilot Communities
Theme:
Dementia Awareness, Community Engagement
Document Type:
Work Plan
Organization / Institution:
Dementia Friendly Communities Project
Author:
Not specified
Target Audience:
Community members, caregivers, employers, and general public
Period of Validity:
Ongoing
Approval Date:
Not specified
Date of Modifications:
Not specified
Year:
2023-2025
Region / City:
Lambeth
Thematic Area:
Child rights, community engagement, youth services
Document Type:
Action Plan
Organization:
Lambeth Borough Council
Author:
Not specified
Target Audience:
Local government officials, youth services, community organizations, elected representatives
Period of Validity:
2023-2025
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2025
Note:
Region / City
Subject:
Baby Friendly Initiative, Maternity Care
Document Type:
Audit Form
Organisation:
Baby Friendly Initiative
Target Audience:
Maternity facilities, health professionals
Period of validity:
Annual
Year:
2016
Region / City:
Lahore, Punjab, Pakistan
Subject:
Solid Waste Management
Document Type:
Tender / Bidding Document
Organization / Institution:
Board of Management Sundar Industrial Estate (BOM-SIE)
Author:
Environment Officer, BOM-SIE
Target Audience:
EPA approved waste management companies and consortiums
Contract Duration:
Minimum one year, extendable by mutual consent
Project Cost:
Approx. Rs. 8,400,000 per annum
Scope:
Door to door collection, transportation, and environmentally friendly disposal of industrial solid waste
Waste Composition:
Paper, plastic, cloth, organic and kitchen waste
Number of Units Covered:
140–150 industrial units daily
Submission Deadline:
14-07-2016 11:00 AM
Bid Opening:
14-07-2016 11:30 AM
Safety Requirements:
PPE including safety shoes, face mask, leather gloves, goggles
Child Labor:
Strictly prohibited
Number of Bins:
450 solid waste bins at 150 points with color coding (Red = Organic, Blue = Paper, Yellow = Plastic + Metals)
Year:
2024
Region / City:
Thurrock, Essex, UK
Type of document:
Community support schedule
Target audience:
People living with dementia and their carers
Locations:
Grays, Chadwell St Mary, Chafford Hundred, Stanford-le-Hope, Tilbury, South Ockendon, Stifford Clays, Bulphan, Orsett, Laindon, Benfleet, Basildon
Activities:
Support groups, coffee mornings, exercise classes, creative activities, lunch clubs, day centres
Cost:
Free or nominal fee for some activities
Contact information:
Multiple emails and phone numbers listed per group
Service period:
Weekly, biweekly, monthly events, specific dates listed
Year:
2021
Organization:
Dubai Healthcare City Authority
Program:
Excellence Awards 2021
Award Category:
People of Determination – Friendly Entity Award
Document Type:
Award Entry Form
Submission Deadline:
May 20, 2021
Interview Period:
1–10 June 2021
Submission Method:
Email submission with required attachments
Maximum Main Document Length:
25 pages including evidence
Maximum Supporting Documents Length:
10 pages including recent CV
Maximum File Size:
40 MB
Target Applicants:
Organizations within DHCC
Required Information:
Applicant details, organizational profile, achievements, accessibility initiatives, community impact, results and outcomes
Consent Requirement:
Agreement to Terms and Conditions and consent for marketing use of submitted materials
Note:
Year
Context description:
Application form for organizations applying for the UNICEF UK Baby Friendly accreditation, including detailed sections for different health services.
Year:
2021
Region / city:
N/A
Subject:
Hospital Accreditation
Document type:
Application Form
Institution:
Quality and Accreditation Institute (QAI), Centre for Accreditation of Health & Social Care (CAHSC)
Author:
N/A
Target audience:
Hospitals applying for accreditation
Period of validity:
N/A
Approval date:
N/A
Date of changes:
March 2021
Year:
2016
Region / City:
Not specified
Subject:
Technology, Hardware
Document Type:
Technical Specification
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Professionals in IT, Security Systems
Effective Period:
Not specified
Approval Date:
2016.07
Modification Date:
Not specified
Year:
Not specified
Region / State:
Washington State
Country:
United States
Program Name:
Breastfeeding Friendly Washington
Managing Authority:
Washington State Department of Health
Program Type:
Voluntary recognition program
Subject:
Breastfeeding support practices in free standing birth centers
Recognition Levels:
Bronze, Silver, Gold
Standards Basis:
Ten Steps to Successful Breastfeeding (World Health Organization)
Related Initiative:
Baby-Friendly® Hospital Initiative
Application Requirements:
Written breastfeeding policy, staff training records, in-service and orientation documentation, Electronic Medical Records, supporting protocols
Submission Contact:
[email protected]
Mailing Address:
PO Box 47830, Olympia, WA 98504-7886
Target Institutions:
Free standing birth centers in Washington State
Evaluation Timeline:
Acknowledgment within one week; review within one month; recognition package within two months if approved
Data Requested:
Total annual births; staffing details for licensed midwives and certified nurse midwives; facility contact and social media information
Authorization Requirement:
Signature confirming accuracy of submitted information
Year:
2014
Region / City:
Bristol
Theme:
Urban Planning, Age-Friendly Cities
Document Type:
Working Paper
Organization / Institution:
Graduate School of Education, University of Bristol
Authors:
Keri Facer, Lindsey Horner, Helen Manchester
Target Audience:
Urban planners, policymakers, researchers, community groups, and the general public
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Context:
The document discusses the concept of an "All-Age Friendly City," focusing on intergenerational design and its importance for both children and older adults.
Year:
2021
Region / City:
N/A
Topic:
Health & Safety, COVID-19 Protocols
Document Type:
Checklist
Organization / Institution:
N/A
Author:
N/A
Target Audience:
Home and away team COVID-19 compliance officers, coaches, players, first aiders
Period of validity:
N/A
Date of approval:
N/A
Date of amendments:
N/A
Note:
Year
Topic:
Environmental Responsibility
Document Type:
Statement
Target Audience:
Guests
Context Description:
A statement by the owners of an accommodation regarding their environmental practices and commitment to sustainability, inviting guests to participate in eco-friendly actions during their stay.
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