№ lp_2_3_52302
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This document is a response to a public consultation regarding the proposed registration standards for paramedics in Australia, focusing on the "grandparenting" provisions and related issues.
Organisation name:
La Trobe University
Registration standard:
Grandparenting
Feedback type:
Public consultation response
Date of submission:
8 February 2018
Jurisdiction:
Australia
Type of document:
Consultation response
Target audience:
Stakeholders in paramedicine regulation
Period of relevance:
2017-2018
Subject:
Paramedicine registration standards
Stakeholders:
Australian health professionals, educational institutions, paramedics
Professional focus:
Paramedicine regulation, qualifications, grandparenting provisions
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Year:
2018
Region / City:
Queensland, Australia
Topic:
Health, Paramedicine, Professional Standards
Document Type:
Submission
Organization / Institution:
Queensland Nurses and Midwives’ Union
Author:
Queensland Nurses and Midwives’ Union
Target Audience:
Paramedicine Board of Australia, Healthcare Professionals
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Context:
Submission on proposed mandatory registration standards for the paramedicine profession to the Paramedicine Board of Australia.
Year:
2020
Jurisdiction:
New Zealand
Legislation:
Education and Training Act 2020
Section:
75
Subject:
School enrolment zones and sibling provisions
Type of document:
Legal guidance / statutory interpretation
Issuing authority:
Ministry of Education
Definitions included:
Sibling, home zone
Applicable to:
Students enrolling in schools with new enrolment schemes
Conditions:
Out-of-zone student enrolment, sibling enrolment, home zone recognition
Year:
2026
Region / city:
United Kingdom
Topic:
Good Manufacturing Practice, Advanced Therapy Medicinal Products (ATMPs)
Document type:
Consultation response
Organization / institution:
NHS Advanced Therapy Medicinal Products Working Party
Author:
Anne Black
Target audience:
Pharmaceutical professionals, regulatory bodies, academic researchers
Period of validity:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
2019
Region / City:
European Union
Topic:
PRIIPs Regulation amendments
Document Type:
Consultation Paper
Institution:
European Supervisory Authorities (ESAs)
Author:
European Supervisory Authorities (ESAs)
Target Audience:
Stakeholders in financial services and investments
Action Period:
16 October 2019 - 13 January 2020
Approval Date:
16 October 2019
Amendment Date:
Not specified
Year:
2026
Region / City:
Greater Manchester
Theme:
Healthcare, Pharmaceutical Recommendations
Document Type:
Report
Institution:
NHS Greater Manchester Medicines Management Group (GMMMG)
Author:
CRG (Clinical Reference Group)
Target Audience:
Healthcare professionals in the NHS
Period of validity:
Until 27th February 2026 (for specific drugs)
Approval Date:
13th January 2026
Date of Changes:
27th February 2026
Cost Impact:
£61,000 per year
Service Implications:
Transfer of prescribing to primary care, potential reduction in specialist service burden
Description:
Recommendations by the Clinical Reference Group (CRG) for the inclusion, continuation, or discontinuation of specific drugs, including azathioprine suspension and sotrovimab, in the Greater Manchester formulary.
Year:
2016
Region / City:
Australia
Topic:
Pharmacy, Medicine Compounding
Document Type:
Consultation Response
Organization:
Pharmaceutical Society of Australia
Author:
Dr Lance Emerson, Chief Executive Officer
Target Audience:
Pharmacists, Pharmacy Regulators
Period of Validity:
Indefinite
Approval Date:
1 February 2016
Date of Amendments:
None
Contextual Description:
Document is a public consultation response discussing terminology issues and proposed updates regarding compounded parenteral medicines, primarily aimed at Australian pharmacists.
Year:
2019
Region / City:
Australia
Topic:
Recency of Practice for Registered Health Practitioners
Document Type:
Consultation Report
Organization / Institution:
National Boards (Aboriginal and Torres Strait Islander Health Practice Board of Australia, Chinese Medicine Board of Australia, Occupational Therapy Board of Australia)
Author:
National Boards
Target Audience:
Registered Health Practitioners
Period of Validity:
2019
Approval Date:
Not specified
Amendment Date:
Not specified
Context:
A consultation report detailing the review of recency of practice (RoP) registration standards for health practitioners in Australia, aiming to establish revised requirements to ensure ongoing professional competence.
Date:
16 October 2019
Organization:
European Supervisory Authorities (ESAs)
Document type:
Response form
Related regulation:
Commission Delegated Regulation (EU) 2017/653
Country/Region:
European Union
Deadline for responses:
13 January 2020
Confidentiality:
Optional, subject to ESAs rules
Respondent:
German Association of Actuaries (DAV)
Activity sector:
Insurance and Pension
Association representation:
Yes
Purpose:
Comments on proposed amendments to PRIIPs KID
Content focus:
Transparency, comparability, and methodology of PRIIPs pre-contractual documents
Source type:
Consultation response
Year:
2019
Region / City:
Europe
Topic:
PRIIPs Regulation, Digital Solutions, KID
Document Type:
Consultation Response
Organization / Institution:
European Supervisory Authorities (ESAs)
Author:
Association Française de la Gestion financière (AFG)
Target Audience:
Financial Industry Stakeholders
Period of Validity:
Until 13 January 2020
Date of Approval:
16 October 2019
Date of Amendments:
Not specified
Year:
2026
Region / City:
United Kingdom
Topic:
Transmission Connection Asset Charging
Document Type:
Consultation Response Proforma
Organ / Institution:
NESO
Author:
Not specified
Target Audience:
Industry parties
Period of validity:
Until 18 February 2026
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Region/City:
North Carolina
Topic:
NEPA/SEPA Consultation Process for Transportation Projects
Document Type:
Form
Agency/Organization:
North Carolina Department of Transportation (NCDOT)
Author:
NCDOT
Target Audience:
NCDOT staff, project managers, consultants
Period of Validity:
Ongoing, applicable as of the date of approval
Approval Date:
Not specified
Date of Changes:
Not specified
Date:
19 November 2025
Organization:
Medicines, Formulary, and Guidelines Group
Location:
Humber and North Yorkshire, UK
Document type:
Consultation summary / Recommendations
Drug:
MV140 Uromune Sublingual vaccine spray
Indication:
Recurrent lower urinary tract infections in adults
Formulary status:
Red – Specialist urology only
Treatment protocol:
2 sprays sublingually once daily for 3 months, possible rechallenge after 18 months
Cost per patient:
£297.50
Monitoring:
Telephone reviews at 1, 3, 6, 9, 12 months; Consultant Urologist review at 6 and 12 months
Professional target audience:
NHS healthcare professionals
Source:
HNY APC Professional Secretariat, Regional Drug and Therapeutics Centre
Year:
2025
Region / City:
United Kingdom
Subject:
Electricity Regulation, Charging Methodology
Document Type:
Consultation Response Form
Organization:
NESO
Author:
Not specified
Target Audience:
Industry parties, Transmission System Operators, Energy Sector Stakeholders
Validity Period:
From 1st April 2026
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2024
Region / City:
Ohio, United States
Subject:
Youth homelessness, Continuum of Care, Housing services, Policy recommendations
Document Type:
Request for Proposals
Organization / Institution:
Coalition on Homelessness and Housing in Ohio (COHHIO)
Author:
Coalition on Homelessness and Housing in Ohio
Target Audience:
Service providers, consultants, organizations focused on youth homelessness, policymakers
Effective Period:
October 29, 2025 - June 30, 2026
Approval Date:
October 29, 2025
Date of Last Revision:
Not provided
Year:
2025
Region / city:
Ghana
Theme:
Electronic communications, broadcasting, digital services
Document type:
Bill
Organization:
National Communications Authority
Author:
National Communications Authority
Target audience:
Licensed service providers, industry stakeholders, civil society organizations, consumers, general public
Period of validity:
From 16th October 2025 to 29th October 2025
Approval date:
16th October 2025
Amendment date:
N/A
Year:
2024
Region / City:
UK
Topic:
Strategy, Optical Professions, Consultation
Document Type:
Consultation Document
Organization / Institution:
General Optical Council
Author:
General Optical Council
Target Audience:
Optical professionals, stakeholders in the eye care sector, policy makers
Effective Period:
1 April 2025 to 31 March 2030
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2024
Region / city:
Ireland
Topic:
Disability, Public Consultation
Document type:
Report
Organization / institution:
National Disability Authority
Author:
National Disability Authority
Target audience:
Disabled persons, government entities, disability organizations
Effective period:
N/A
Approval date:
N/A
Date of amendments:
N/A
Year:
2023
Region / City:
N/A
Topic:
Registration Service, Operational Choreography
Document Type:
Change Request
Organization:
MHHS Programme
Author:
N/A
Target Audience:
Programme Participants
Period of Validity:
N/A
Approval Date:
08/02/2023
Date of Changes:
N/A
Document type:
Process note
Subject:
Elog electronic authentication for UCC and transaction eligibility
Applicable order types:
Lumpsum purchase, spread fresh purchase without folio, SIP, XSIP, ISIP fresh registrations without folio, redemption, switch
Mode of holding:
Single, joint, anyone or survivor
DP transaction type:
Non-demat, demat
Scope:
UCC creation, AOF handling, Elog authentication
Applicable entities:
Members, investors, RTAs
Authentication channels:
Email, SMS, API
Authentication validity period:
5 working days from UCC creation
Tax status applicability:
Individual and non-individual categories with Elog eligibility
Transaction condition:
Mandatory Elog or AOF for non-demat order placement
Regulatory context:
Mutual fund transactions and systematic registrations
Year:
2023
Region / City:
New Zealand
Topic:
Food Certification
Document Type:
Application Form
Organization:
Ministry for Primary Industries
Author:
Not specified
Target Audience:
Exporters of non-animal derived food products to Thailand
Period of Validity:
5 years
Approval Date:
Not specified
Date of Changes:
Not specified