№ lp_2_1_30139
File format: docx
Character count: 3738
File size: 72 KB
Structured administration document authorizing registered pharmacists in Western Australia to supply specific oral antibiotics to adult female patients with uncomplicated urinary tract infections under defined training and clinical conditions.
Year:
2023
Region:
Western Australia
Type of document:
Structured Administration and Supply Arrangement (SASA)
Authority:
Chief Executive Officer of Health under Part 6 of the Medicines and Poisons Regulations 2016
Issuer:
Dr Andrew Robertson, Chief Health Officer, Department of Health WA
Practitioner:
Registered Pharmacists with approved training
Practice setting:
Registered community pharmacies in Western Australia
Approved activity:
Supply of Schedule 4 oral antibiotics for uncomplicated urinary tract infection
Approved medicines:
Nitrofurantoin, Trimethoprim
Target population:
Female patients aged 18–65 with uncomplicated UTI
Conditions:
Compliance with training, registration, clinical criteria, record-keeping, and regulatory requirements
Date issued:
24 July 2023
Contact:
Medicines and Poisons Regulation Branch, [email protected]
Note:
, Number 034/7-2023
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2025
Region / city:
Victoria, Australia
Topic:
Health, Urinary Tract Infection, Pharmacist Services
Document type:
Patient handout
Author:
Department of Health, Victoria Government
Target audience:
Women and gender diverse people with female biology aged 18-65, including Medicare and international students
Period of validity:
December 2025
Approval date:
December 2025
Date of updates:
Not specified
Year:
2024
Region / city:
Victoria, Australia
Topic:
Urinary Tract Infection Treatment
Document Type:
Patient Handout
Organ / Institution:
Department of Health, Victoria
Author:
Department of Health, Victoria
Target Audience:
Women and gender diverse people with female biology aged 18-65
Period of validity:
March 2024
Approval date:
March 2024
Date of amendments:
N/A
Contextual Description:
Patient handout providing details about treatment, eligibility, and self-care for uncomplicated urinary tract infection under a pilot program for community pharmacists.
Year:
Not specified
Region / City:
Not specified
Subject:
Acute uncomplicated urinary tract infection (UTI) treatment
Document Type:
Patient Group Direction (PGD)
Author:
Not specified
Target Audience:
Healthcare professionals, community pharmacy staff
Effective Period:
Not specified
Approval Date:
Not specified
Revision Date:
Not specified
Year:
N/A
Region / City:
N/A
Subject:
Acute Urinary Tract Infection Treatment
Document Type:
Patient Group Direction
Organization / Institution:
N/A
Author:
N/A
Target Audience:
Healthcare professionals, pharmacists
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Organisation:
Canberra Health Services
Document type:
Guideline
Reference number:
CHS25/225
Jurisdiction:
Australian Capital Territory
Healthcare setting:
Public health services
Subject area:
Medication management
Professional scope:
Nursing and midwifery practice
Approved by:
Drug and Therapeutics Committee
Target professionals:
Registered nurses and registered midwives
Patient groups:
Adults, children 12 years or older, and selected medicines for children under 12 years
Exclusions:
Neonates, Special Care Nursery patients, Neonatal Intensive Care Unit patients
Regulatory framework:
Australian medicines scheduling (Schedules 2, 3, 4, and 8)
Content components:
Governance, safe use, documentation, approved medicine lists
Year:
2025
Region / city:
Netherlands
Topic:
Clinical Trials, Industry, Medicine
Document Type:
Agreement
Institution:
Nationale Federatie van Universitair Medische Centra (NFU), vereniging Samenwerkende Topklinische opleidingsZiekenhuizen (STZ), Vereniging Innovatieve Geneesmiddelen, Stichting Het Nederlands Kanker Instituut - Antoni van Leeuwenhoek Ziekenhuis (NKI/AvL), Prinses Máxima Centrum voor Kinderoncologie, Associatie van Contract Research Organisaties in Nederland (ACRON)
Author:
Not specified
Target audience:
Sponsors, CROs, Research Institutions
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Context:
A template for clinical trial agreements between industry sponsors, academic and non-academic hospitals in the Netherlands, including protocols, financial arrangements, and data protection requirements.
Year:
2023-2025
Region / City:
N/A
Subject:
Tenure Review Process
Document Type:
Procedural Guide
Institution:
N/A
Author:
Michael Susi, Jessie Tong, Margaret Edsall, Angel Flesher, Eugenia Lean, Mary Boyce
Target Audience:
Faculty members undergoing tenure review
Period of Validity:
2023-2025
Approval Date:
N/A
Date of Modifications:
N/A
Year:
2021
Region / City:
Not specified
Topic:
Patient follow-up process
Document Type:
Standard Operating Procedure (SOP)
Issuing Organization:
Not specified
Author:
Kirstin Eadie
Target Audience:
Clinical and administrative staff, operational managers, BI team
Effective Period:
Not specified
Approval Date:
27th September 2021
Date of Changes:
Not specified
State:
New Jersey
Country:
United States
Issuing body:
New Jersey Department of Education, Division of Teaching and Learning Services
Legal reference:
N.J.A.C. 6A:8-2.1
Standards last adopted:
2020
Review process initiated:
May 2025
Subject area:
Career readiness, financial literacy, information literacy, key competencies
Education levels:
Kindergarten through Grade 12
Domains:
Career Readiness; Personal Financial Literacy; Information Literacy; Key Competencies and Skills
Document structure:
Framework, disciplinary concepts, developmental progressions, performance expectations by grade band, summary of changes
Type of document:
State educational standards framework
Year:
2020
Region / city:
N/A
Topic:
Network procedure correction
Document type:
Change Request
Organization:
3GPP
Author:
Mediatek Inc.
Target audience:
Technical experts and network engineers
Effective period:
N/A
Approval date:
2020-06-08
Modification date:
N/A
Release:
Rel-16
Work item code:
TEI16
Category:
F
Clauses affected:
5.5.2.3.5
Summary:
The change request proposes a correction to the handling of abnormal cases in network initiated detach procedures, specifically addressing synchronization issues between the network and UE.
Year:
2025
Region / city:
Zurich
Theme:
Oncology, Clinical Trials
Document Type:
Funding Proposal
Institution:
University of Zurich, CCCZ
Author:
N/A
Target Audience:
Researchers, Investigators, Clinical Trials Applicants
Validity Period:
2025
Approval Date:
N/A
Date of Changes:
N/A
Context:
Detailed proposal outline for a research funding call for investigator-initiated clinical trials in oncology, including project description, team structure, cost estimate, and timelines.
Year:
2021
Region / City:
Canberra
Subject:
Surgery, Postponement, Elective Surgery
Document Type:
Standard Operating Procedure
Organization:
Canberra Health Services
Author:
Policy Team
Target Audience:
Medical Officers, Registered Nurses, Management/Executive Officers
Period of Validity:
Not specified
Approval Date:
12 November 2021
Amendment Date:
Not specified
Related Policies:
Elective Surgery Access, Clinical Records Management, Informed Consent, Occupational Violence, Consumer Feedback Management
Evaluation:
Monthly reviews of all elective surgery postponements
Legislation:
Health Records (Privacy and Access) Act 1997, Human Rights Act 2019, Work Health and Safety Act 2011
References:
Elective Surgery Access and Management Policy (2021), Waiting Time and Elective Surgery Policy (2012), Elective Surgery Access Policy (2015)
Search Terms:
Postponement, Surgery, Elective, Rescheduling, Elective Waiting List
Contextual Description:
This is a procedural document outlining the steps and guidelines for hospital-initiated postponement and rescheduling of elective surgeries at Canberra Health Services.
Type of Document:
Clinical Trial Research Agreement
Jurisdiction:
Australia
Parties:
Institution and Organisation
Subject:
Investigator Initiated Study
Related Legislation:
Privacy Act 1988 (Cth); A New Tax System (Goods and Services Tax) Act 1999 (Cth)
Regulatory Authorities:
Therapeutic Goods Administration (TGA); National Health and Medical Research Council (NHMRC)
Applicable Guidelines:
ICH Good Clinical Practice (CPMP/ICH/135/95) as adopted by TGA
Scope:
Conduct of a clinical study in accordance with an approved Protocol
Key Roles:
Principal Investigator; Responsible Human Research Ethics Committee (HREC)
Confidentiality:
Protection of Confidential Information excluding Personal Information
Intellectual Property:
Allocation and definition of Background and Study-related Intellectual Property
Study Components:
Protocol; Investigator’s Brochure; Case Report Forms; Biological Samples; Investigational Product
Completion Criteria:
Database lock and provision of Essential Documents including HREC acknowledgment
Year:
2021
Region / City:
United Kingdom
Topic:
Healthcare, Patient Care
Document Type:
Standard Operating Procedure (SOP)
Institution:
NHS
Author:
National Health Service (NHS)
Target Audience:
Healthcare professionals
Period of Application:
Indefinite
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Region / City:
Sacramento, California
Theme:
Public Utilities Commission, Regulatory Procedures, Utility Applications
Document Type:
Resolution
Institution / Organization:
Public Utilities Commission of the State of California
Author:
Public Utilities Commission of the State of California
Target Audience:
Utility companies, legal and regulatory professionals, public servants
Period of Validity:
Ongoing
Approval Date:
February 5, 2026
Amendment Date:
Not specified
Year:
2026
Region / City:
University of the Witwatersrand, South Africa
Subject:
Human Research Ethics
Document Type:
Application Form
Institution:
Human Research Ethics Committee (Medical)
Target Audience:
Researchers seeking ethics waiver
Purpose:
Postgraduate or investigator-initiated research without active human participation
Submission Method:
Email to Medical Ethics Office
Requirements:
Completion of all sections, typed form, ethics training certificate attached
Data Collection:
Not permitted before ethics clearance
Study Categories:
Literature review, in vitro study, microbiology, environmental surveillance, public observation
Applicant Roles:
Principal Investigator, Co-Investigator, Supervisor, Applicant
Endorsements:
Department/Unit Head, Academic or Clinical Head approval required
Guidelines Reference:
Appendix to the HREC (Medical) Application Form
Year:
2026
Institution:
University of Memphis Cecil C. Humphreys School of Law
Document Type:
Form
Audience:
Law students
Purpose:
Approval of student-initiated pro bono projects
Requirements:
Compliance with Pro Bono Handbook, prior approval before service
Submission:
Individual or group submission with participant list
Supervisor:
Anticipated organization supervisor contact information required
Project Scope:
Description of direct legal services and pro bono qualification
Training:
Indicate if training will be provided
Additional Notes:
Space for extra comments
Year:
2018
Region / City:
Victoria, Australia
Topic:
Education, Community Development
Document Type:
Guidelines
Organization:
Adult, Community and Further Education (ACFE) Board
Author:
ACFE Board
Target Audience:
Registered Learn Local Providers, Adult Education Institutions
Period of Validity:
2018-2019
Approval Date:
Not specified
Date of Changes:
Not specified
Country:
New Zealand
City:
Christchurch
Institution:
Christchurch Hospital
Organisation:
Nursing Council New Zealand; Canterbury District Health Board
Document Type:
Clinical agreement
Subject:
Nurse-initiated radiology referrals for adult patients
Healthcare Field:
Radiology; Nursing practice
Authorising Roles:
Clinical Director / Chief of Service; Chief of Radiology; Director of Nursing
Target Audience:
Clinical Nurse Specialists; Senior Medical Officers; Registered Medical Officers; Charge Nurse Managers; Radiologists; MRTs; Radiology nursing staff
Applicable Staff:
Registered Nurses and Nurse Practitioners registered with the Nursing Council New Zealand
Scope:
Adult patients within the specified hospital service
Associated Policies:
Midwife, Nurse Practitioner and Nurse Initiated Radiology Referrals Policy; CDHB Radiation Safety Plan
Associated Forms:
Diagnostic Radiology Consultation Form (QF00294); Interventional Radiology Consultation Form (QF01157)
Training Requirement:
CDHB healthLearn Nurse Midwife Radiology Referrals programme
Legal Reference:
Radiation Protection Act
Oversight:
Clinical Director of the service; Chief of Radiology; Director of Nursing
Audit Requirement:
Annual audit of nurse-initiated radiology referrals
Approval Process:
Clinical Director / Chief of Service; Chief of Radiology; Director of Nursing
Agreement Owner:
Clinical Director of the service; Director of Nursing
Authoriser:
Chief of Radiology (Principal Licence Holder)
Date of Authorisation:
dd month 20xx