№ files_lp_3_process_7_075281
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Checklist for submitting documents to renew or amend Authorised Prescriber approval under NIIM HREC regulations, including required forms, supporting evidence, and declarations.
Year:
2026
Region / City:
Australia
Subject:
Authorised Prescriber Approval Renewal and Amendments
Document Type:
Application Checklist / Form
Organization:
NIIM HREC
Author:
Not specified
Target Audience:
Healthcare professionals seeking Authorised Prescriber approval
Effective Period:
Ongoing until next renewal
Date of Issue:
2026
Attachments Required:
Renewal and Amendment Form, Original NIIM HREC Approval Letter, Amendment Letters (if applicable), Evidence of Continuing Professional Education, Product Information, Proof of Payment
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
Not specified
Region / city:
Not specified
Topic:
Medical Assessment, Bed and Mattress Management
Document Type:
Assessment Form
Organization / Institution:
SWEP
Author:
SWEP Clinical Advisors
Target Audience:
Healthcare professionals, caregivers
Period of validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Document Type:
Letter
Target Audience:
Primary Care Prescriber
Year:
2026
Country:
Australia
Type of document:
Application form
Issuing authority:
Therapeutic Goods Administration (TGA)
Intended audience:
Medical practitioners
Purpose:
Application to become an authorised prescriber of unapproved medicines or medical devices
Regulatory reference:
Therapeutic Goods Regulations 1990, Regulation 12B(1B)
Required attachments:
Ethics committee or specialist college approval/declaration (if applicable)
Information collected:
Personal details of medical practitioner, patient consent, product information, prescribing details
Submission method:
Email or fax to TGA
Year:
Not specified
Region / City:
Not specified
Topic:
Medicine Prescriber Category Change
Document Type:
Form
Institution:
Ministry of Health (MOH)
Author:
Not specified
Target Audience:
Healthcare professionals involved in prescribing medicines
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Contextual Description:
Form for proposing changes to the prescriber category of medicines in the Ministry of Health Medicines Formulary, including necessary information about the medicine, dosage, and rationale for the change.
Year:
1993
Region / City:
Massachusetts
Subject:
Nursing Practice
Document Type:
Advisory Ruling
Authority:
Massachusetts Board of Registration in Nursing
Target Audience:
Registered Nurses, Licensed Practical Nurses
Period of Validity:
Ongoing
Approval Date:
September 22, 1993
Revision Dates:
July 10, 2002; December 9, 2009; October 8, 2014; April 11, 2018
Year:
2023
Region / City:
Humber & North Yorkshire
Topic:
Healthcare, Community Pharmacy, Data Privacy
Document Type:
Programme Description
Organization / Institution:
NHS England, Humber & North Yorkshire Integrated Care Board
Author:
NHS England
Target Audience:
Healthcare professionals, community pharmacies
Period of Implementation:
April 2023 – April 2025
Approval Date:
Not specified
Modification Date:
Not specified
Year:
1989
Region / City:
Australia
Topic:
Therapeutic Goods
Document Type:
Application Form
Organization / Institution:
HREC
Author:
Unknown
Target Audience:
Medical practitioners, HREC members
Effective Period:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2023
Region / city:
Australia
Topic:
Psychedelic-assisted therapy, psilocybin
Document type:
Application form
Organization:
Therapeutic Goods Administration (TGA), National Institute of Integrative Medicine (NIIM)
Author:
Not specified
Target audience:
Registered psychiatrists seeking approval to prescribe psilocybin
Validity period:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
2023
Region / Country:
Australia
Subject:
Nursing and midwifery practice regulation
Document type:
Consultation Regulation Impact Statement (C-RIS)
Issuing body:
Nursing and Midwifery Board of Australia (NMBA)
Authors / Contributors:
Registered Nurse Prescribing Working Group, NMBA
Target audience:
Healthcare professionals, policymakers, stakeholders in nursing and midwifery
Consultation period:
16 June 2023 – 28 July 2023
Related documents:
NMBA Registration Standards, ANMAC Endorsed Midwife Accreditation Standards, Health Workforce Australia HPPP Project Report, NPS Prescribing Competency Framework
Purpose:
Evaluate regulatory impacts of proposed nurse prescribing registration standard
Submission method:
Email to [email protected]
Note:
in Word format
Decision-making process:
Feedback reviewed to develop Decision RIS for Ministerial approval
Summary:
Evaluative government source analyzing options for implementing designated registered nurse prescribing and consulting stakeholders on regulatory impacts.
Organisation:
Melksham and Bradford on Avon Primary Care Network (M&BoA PCN)
Job title:
Social Prescriber Link Worker (SPLW)
Line manager:
Social Prescribing Development Lead
Accountable to:
PCN Network Manager
Hours per week:
Flexible up to full-time (37.5 hours)
Salary:
£15.20 – £15.32 per hour
Location:
Bradford on Avon and Melksham, United Kingdom
Population covered:
Approximately 48,000 patients
Participating practices:
Bradford on Avon & Melksham Health Partnership; Giffords Surgery; Spa Medical Centre
Team structure:
Wellbeing Team including Health Coaches, Social Prescribing Link Workers and Care Coordinators
Target population:
Adults aged 18 years and over, including older people
Employment sector:
Primary Care / General Practice
Service focus:
Social prescribing and community-based wellbeing support
Legislative framework:
Health and Safety at Work Act 1974; Environmental Protection Act 1990; Environment Act 1995; Fire Precautions (Workplace) Regulations 1999; Coronavirus Act 2020
Core principles:
Equality, Diversity and Inclusion; Confidentiality; Quality and Continuous Improvement; Safety, Health, Environment and Fire (SHEF)
Referral system:
GP clinical systems using national SNOMED codes
Induction requirement:
Full induction within M&BoA PCN and member practices
Training requirement:
Mandatory training as directed by Host Practice
Year:
2026
Country:
Australia
Document type:
Fact sheet
Regulatory body:
Nursing and Midwifery Board of Australia (NMBA)
Subject:
Endorsement for scheduled medicines for registered nurses
Target audience:
Registered nurses in Australia seeking endorsement
Effective date:
30 September 2025
Requirements:
NMBA-approved postgraduate education, 5,000 hours of clinical experience, clinical mentorship
Scope:
Administration, possession, prescribing, supply, and use of Schedule 2, 3, 4, and 8 medicines under prescribing agreements
Related legislation:
Health Practitioner Regulation National Law, state and territory medicines and poisons legislation, Therapeutic Goods Administration regulations
Year:
2022
Region / City:
Not specified
Subject:
Nuclear safety, regulatory compliance
Document Type:
Technical Guide
Organization:
Office for Nuclear Regulation (ONR)
Author:
Nuclear Equivalence Inspector
Target Audience:
ONR inspectors, licensees
Period of Validity:
Until Dec-2025
Approval Date:
Dec-2022
Revision Date:
Not specified
Document Reference:
NS-INSP-GD-012
Record Reference No.:
2022/72622
Year:
2017-2020
Region / City:
Ballymount, Dublin
Theme:
Waste Management
Document Type:
Application Form
Organization:
Circol ELT Ltd
Author:
Circol ELT Ltd
Target Audience:
Waste collectors, companies seeking registration
Period of validity:
2017-2020
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Country:
Australia
Type of document:
Application form
Issuing authority:
Therapeutic Goods Administration (TGA)
Intended audience:
Medical practitioners
Purpose:
Application to become an authorised prescriber of unapproved medicines or medical devices
Regulatory reference:
Therapeutic Goods Regulations 1990, Regulation 12B(1B)
Required attachments:
Ethics committee or specialist college approval/declaration (if applicable)
Information collected:
Personal details of medical practitioner, patient consent, product information, prescribing details
Submission method:
Email or fax to TGA
Year:
2024
Region / City:
European Union
Topic:
Vehicle Authorization, Regulatory Changes
Document Type:
Notification Form
Agency:
European Union Agency for Railways
Author:
European Commission
Target Audience:
Entities managing vehicle authorization changes
Period of Validity:
From 1 October 2024
Approval Date:
Not specified
Date of Changes:
1 October 2024
Context:
A notification form used by entities to inform the European Union Agency for Railways about changes to an already authorized vehicle, following regulatory guidelines and requirements for new authorizations under EU regulations.
Year:
2023
Region / City:
European Union
Topic:
Clinical Trials, Medical Regulation
Document Type:
Cover Letter
Organization:
European Commission
Author:
European Commission
Target Audience:
Pharmaceutical Companies, Clinical Trial Sponsors
Action Period:
Transition of Clinical Trials from Directive 2001/20/EC to Regulation (EU) No 536/2014
Approval Date:
N/A
Amendment Date:
N/A
Year:
2015
Type of document:
Assessment report template
Subject:
Pharmacovigilance, Periodic Safety Update Reports (PSUR)
Organization:
European Medicines Agency (EMA)
Target audience:
Lead Member States, MAHs, PRAC members
Procedure number:
Not specified
Data lock point:
Not specified
Status:
Guidance and procedural template
References:
GVP Module V, VII, VIII; Variations Classification guideline Commission Regulation 1234/2008; HMA/EMEA recommendations EMEA/743133/2009