№ files_lp_4_process_3_112527
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Structured competency assessment checklist used within the Nursing Council of New Zealand portfolio review process documenting evidence and verification of professional practice, education, and competency standards for Registered Nurses.
Document Type:
Portfolio assessment checklist
Professional Field:
Nursing
Purpose:
Verification of competency requirements for Registered Nurse portfolio
Regulatory Body:
Nursing Council of New Zealand (NCNZ)
Related Program:
Professional Development and Recognition Programme (PDRP)
Target Profession:
Registered Nurses
Assessment Method:
Portfolio evidence review
Required Evidence:
Application letter, role description, APC copy, self and peer assessment, practice hours verification, professional development records, reflections, competency evidence
Minimum Practice Requirement:
450 practice hours in the last 3 years
Professional Development Requirement:
60 hours in the last 3 years
Key Competency Areas:
Professional responsibility, management of nursing care, interpersonal relationships, interprofessional healthcare collaboration
Associated Principles:
Treaty of Waitangi principles in nursing practice
Assessment Roles:
Portfolio Assessor, Charge Nurse, Nurse Manager, Peer Assessor
Verification Elements:
Signatures, competency confirmation, documentation review
Optional Component:
Curriculum Vitae
Assessment Fields:
Evidence required, compliance status, assessor comments, assessor identification and registration number
Price: 8 / 10 USD
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Year:
2023
Region / city:
New Zealand
Subject:
Nursing practice, health care competencies, professional responsibility
Document type:
Self-assessment form
Organization / institution:
Nursing Council of New Zealand
Author:
Nursing Council of New Zealand
Target audience:
Registered Nurses in New Zealand
Effective period:
April 1, 2025 (change in PDRP peer assessment requirement)
Approval date:
2023
Modification date:
2023
Programme:
Bachelor of Nursing (BN)
Academic Year:
Year 2
Country:
New Zealand
Professional Framework:
Nursing Council of New Zealand (NCNZ) Indicators
Subject Area:
Nursing Education and Professional Competencies
Document Type:
Educational learning outcomes framework
Field:
Nursing Practice and Health Care
Key Topics:
Professional behaviour, legal and ethical practice, Te Tiriti o Waitangi, cultural safety, nursing assessment and care planning, clinical documentation, reflective practice, health education, therapeutic relationships, interdisciplinary collaboration
Related Population:
Health consumers in Aotearoa/New Zealand
Cultural Reference:
Māori health and Te Tiriti o Waitangi principles
Educational Purpose:
Definition of expected competencies and practice indicators for second-year nursing students
Scope of Practice Context:
Undergraduate nursing training aligned with NCNZ professional standards
Year:
2023
Region / City:
European Union
Subject:
Biocidal Products Regulation (EU) No 528/2012
Document Type:
Report
Organization / Institution:
European Chemicals Agency (ECHA)
Author:
European Chemicals Agency (ECHA)
Period of Validity:
Ongoing, with updates from 2015 to 2023
Approval Date:
December 2023
Date of Last Changes:
December 2023
Year:
2011
Region / City:
London
Topic:
Railways, Interoperability, Safety Regulations
Document Type:
Application Letter
Organization:
Department for Transport
Author:
PROJECT ENTITY
Target Audience:
Competent Authority, Rail Interoperability Team
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
2024
Region / city:
Not specified
Topic:
Biocidal products
Document type:
Meeting minutes
Institution:
European Commission
Author:
Not specified
Target audience:
Competent Authorities of EU Member States
Period of validity:
Not specified
Approval date:
Not specified
Date of amendments:
Not specified
Context:
Meeting minutes of the 106th session of the Competent Authorities for the implementation of Regulation (EU) No 528/2012, discussing issues related to biocidal products and their regulation within the EU.
Year:
2024
Region / City:
European Union
Topic:
Biocidal Products, Legislation
Document Type:
Meeting Minutes
Organization / Institution:
European Commission
Author:
European Commission
Target Audience:
Competent Authorities of Member States
Period of validity:
26-27 September 2024
Approval Date:
27 September 2024
Date of amendments:
None
Contextual Description:
Minutes of a meeting of the representatives of Competent Authorities from Member States, discussing the implementation of Regulation (EU) No 528/2012 concerning biocidal products.
Year:
2015
Region / city:
European Union
Subject:
Management of product authorisation for in situ cases
Type of document:
Official guideline
Organization:
European Commission
Target audience:
Competent Authorities, applicants for biocidal product authorisation
Effective period:
Ongoing
Approval date:
23 June 2015
Year:
2023
Region / city:
Brussels
Subject:
Chemicals, Classification, and Labelling
Document Type:
Meeting Record
Organ / institution:
European Commission
Author:
Directorate-General for Environment, Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
Target audience:
Competent Authorities for REACH and CLP
Period of validity:
06/03/2024
Approval date:
06/03/2024
Date of changes:
N/A
Contextual description:
A record of the 50th meeting of the Competent Authorities for REACH and CLP, discussing updates on the Globally Harmonized System, ongoing work on new hazard classes, and the implementation of GHS revisions.
Year:
2023
Region / City:
European Union
Subject:
Biocidal products, Regulation (EU) No 528/2012, Union authorisation
Document Type:
Official Discussion Paper
Authoring Organization:
European Commission
Period of Validity:
Ongoing
Date of Approval:
N/A
Date of Last Revision:
N/A
Year:
2022
Region / City:
Europe
Topic:
Biocidal products
Document Type:
Agenda
Organization / Institution:
Competent Authorities for the implementation of Regulation (EU) No 528/2012
Author:
N/A
Target Audience:
Member States Competent Authorities
Period of Validity:
22-23 June 2022
Approval Date:
N/A
Date of Modifications:
N/A
Date:
28/04/2022
Region / City:
Brussels
Subject:
Polymers, Chemicals Strategy
Document Type:
Background Document
Organization:
European Commission, Directorate-General for Environment
Author:
European Commission
Target Audience:
REACH and CLP Competent Authorities, Environmental Experts
Period of Application:
May 2022
Approval Date:
28/04/2022
Year:
2017
Region / city:
European Union
Subject:
Implementing the concept of biocidal product family
Document type:
Guidance note
Author:
European Commission
Period of validity:
Ongoing
Approval date:
November 2014
Date of changes:
March 2017, July 2017
Keywords:
Biocidal product family, authorisation, regulation, EU, risk assessment, efficacy
Year:
1993
Region / City:
South Africa
Topic:
Occupational Health and Safety
Document Type:
Appointment Letter
Institution:
Employer
Author:
CEO
Target Audience:
Employee
Period of Validity:
Ongoing
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2015
Region / city:
International
Topic:
Medical Device Regulation
Document Type:
Official Report
Organization / Institution:
International Medical Device Regulators Forum (IMDRF)
Author:
National Competent Authority Report Working Group
Target Audience:
Medical Device Regulators, Public Health Authorities
Period of validity:
Ongoing
Approval Date:
26 March 2015
Date of amendments:
None
Year:
2024
Region / city:
EU
Topic:
Biocidal products, PFAS substances, REACH Regulation
Document type:
Regulatory document
Organization / institution:
Competent Authorities of Member States
Author:
Not specified
Target audience:
Competent Authorities, stakeholders in biocidal products regulation
Period of validity:
Not specified
Approval date:
September 2024
Date of changes:
Not specified
Year:
2026
Region / City:
California
Topic:
Forestry, Wildlife Conservation, Timber Harvesting
Document Type:
Guidance Document
Organization:
California Department of Forestry and Fire Protection (CAL FIRE)
Author:
Not specified
Target Audience:
Registered Professional Foresters (RPFs)
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Region / city:
Singapore
Subject:
Legal agreement, Securities, Investment
Document type:
Legal Agreement, Financial Instrument
Institution:
Company incorporated in Singapore
Author:
[Company Name]
Target audience:
Investors, Legal professionals, Financial institutions
Effective period:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
2025
Region / city:
[insert local health board name]
Theme:
Vaccination
Document type:
Patient Group Direction (PGD)
Authorising organisation:
NHS Wales
Target audience:
Healthcare professionals (Registered)
Period of validity:
01 September 2025 - 31 March 2026
Approval date:
07 August 2025
Amendment date:
30 June 2025
Review date:
01 July 2026
Expiry date:
31 March 2026