№ lp_1_20791
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Character count: 26807
File size: 115 KB
Document provides a detailed guide on labelling requirements for alcoholic beverages in accordance with the Australia New Zealand Food Standards Code, including compliance with ingredient listings, claims, and regulatory specifications for different markets.
Year:
2024
Region / City:
New Zealand, Australia
Theme:
Labelling regulations for alcoholic beverages
Document Type:
Regulatory Guidelines
Target Audience:
Brewers, Food and Beverage Industry
Period of Validity:
Ongoing (subject to updates)
Approval Date:
February 2024
Date of Changes:
N/A
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Year:
2023
Region / City:
United Nations
Topic:
Chemicals, Classification, Hazardous Materials
Document Type:
Working Document
Organization / Institution:
United Nations Sub-Committee of Experts on the Globally Harmonized System of Classification and Labelling of Chemicals
Author:
United Nations
Target Audience:
Stakeholders in Canada
Period of validity:
July 10 – 12, 2023
Approval Date:
June 1, 2023
Date of Changes:
N/A
Contextual Description:
A working document listing summaries of proposals and discussions for the 44th session of the UN Sub-Committee of Experts on the Globally Harmonized System of Classification and Labelling of Chemicals, specifically for Canadian stakeholders.
Year:
2012
Region / city:
Kenya
Topic:
Energy Efficiency, Environmental Policy
Document Type:
Mid-Term Evaluation Report
Organization / Institution:
United Nations Development Programme (UNDP)
Author:
Not specified
Target Audience:
Government, environmental organizations, stakeholders in energy efficiency programs
Period of Validity:
2012-2017
Approval Date:
4 September 2012
Date of Changes:
Not specified
Year:
2024
Region / City:
Accra, Ghana
Theme:
Pharmaceutical Labelling
Document Type:
Guideline
Organization / Institution:
Food and Drugs Authority
Author:
Food and Drugs Authority
Target Audience:
Pharmaceutical Manufacturers
Validity Period:
Ongoing
Approval Date:
1st February 2013
Date of Revision:
8th January 2024
Year:
2024
Place:
Brussels
Document reference:
Doc. CA/12/2023 rev. 2
Meeting:
52nd Meeting of Competent Authorities for REACH and CLP (CARACAL)
Session:
Open session
Meeting dates:
1–2 July 2024
Meeting format:
Hybrid
Concern:
CLP classification and labelling of formulations containing micro-encapsulated chemicals
Agenda point:
CLP Open session, AP 7
Action requested:
Discussion and comments
Deadline for written comments:
4 September 2024
Issuing bodies:
European Commission Directorate-General for Environment; Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
Regulatory framework:
CLP Regulation; REACH Regulation
Document status:
Revision 2
Revision history:
Simplification following comments from AT, NL, SE and CropLife Europe
Purpose:
Collection of CARACAL views on classification and labelling approaches
Target group:
Competent authorities under REACH and CLP
Note:
Year
Year:
2010
Region / City:
National (UK)
Theme:
Health, Blood Transfusion, Patient Safety
Document Type:
Competency Assessment Guidelines
Institution:
Skills for Health
Author:
British Society for Haematology, National Patient Safety Agency
Target Audience:
Healthcare Professionals involved in blood transfusion and venepuncture
Period of Validity:
Ongoing (with annual reviews as per local training needs)
Approval Date:
June 2010
Date of Updates:
N/A
Year:
2022
Region / City:
Rwanda, Kigali
Theme:
Chemical safety, labelling
Document type:
Notification
Organ / Institution:
Rwanda Standards Board (RSB)
Author:
Rwanda Standards Board (RSB)
Target audience:
Industry professionals, regulatory bodies
Adoption date:
To be determined
Entry into force date:
To be determined
Final date for comments:
60 days from notification
Year:
2021
Region / City:
Australia
Subject:
Biologicals, Labelling Requirements
Document Type:
Regulatory Guidelines
Organization / Institution:
Therapeutic Goods Administration (TGA)
Author:
Therapeutic Goods Administration (TGA)
Target Audience:
Manufacturers and sponsors of biologicals
Effective Period:
From 30 September 2021
Approval Date:
May 2021
Revision Date:
Not specified
Year:
2017
Region / City:
Moka
Topic:
Conformity report for regulated machinery
Document Type:
Guidelines
Authority / Organization:
Mauritius Standards Bureau
Target Audience:
Importers, dealers
Action Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Note:
Year
Subject:
Clinical Trial Procedures
Document Type:
Standard Operating Procedure
Organization / Institution:
[group/institution]
Target Audience:
Clinical trial team, pharmacy staff
Version Number:
1
Organisation:
Leeds Teaching Hospitals NHS Trust (LTHT)
Hub reference:
PPATH-POL-33
Version:
4.5 (PC103)
Policy Lead:
Dan Carless
Policy Authors:
Ian Cocking; Nicola Millican; Rachel Strafford; Mark Davy; Mark Dunn; Magda Burgess; Carys Lippiatt; Victor Gill; Dan Carless
Approved by:
Executive Team
Responsible Committee/Group:
Pathology CSU Quality Assurance Group
Date of approval:
22 December 2025
Review date:
09 November 2027
Executive Lead:
Chief Medical Office
Target audience:
All staff sending specimens to LTHT Pathology for analysis or storage
Keywords:
Sample; specimen; request form; labelling; acceptance; rejection
Type of document:
Trust policy
Subject:
Labelling and acceptance standards for biological specimens and request forms
Scope:
All locations sending specimens to LTHT Pathology, within and outside the Trust
Policy supersedes:
PPATH-POL-33 v4.5
Year:
Not Applicable
Region / City:
Not Applicable
Topic:
Blood Transfusion, Labelling Procedures
Document Type:
Procedure Manual
Organization / Institution:
Transfusion Medicine and Tissue Bank
Author:
Not Applicable
Target Audience:
Medical staff, Transfusion Medicine professionals
Period of Validity:
Not Applicable
Approval Date:
Not Applicable
Date of Changes:
Not Applicable
Year:
2023
Region / City:
Global
Topic:
Food labelling
Document type:
Quiz
Organization / Institution:
Not specified
Author:
Not specified
Target audience:
General public
Effective period:
Not specified
Approval date:
Not specified
Modification date:
Not specified
Context:
A quiz on food labelling requirements and regulations, intended to test knowledge of food packaging laws and practices.
Year:
2020
Date:
15 October 2020
Closing Date for Submissions:
20 November 2020
Jurisdiction:
Singapore
Issuing Authority:
Singapore Food Agency (SFA)
Document Type:
Consultation paper
Subject:
Labelling requirements for prepacked food
Legal Framework:
Singapore Food Regulations (SFR)
Regulations Covered:
Regulation 5, Regulation 6, Regulation 9, Regulation 9B
International References:
Codex Alimentarius Commission standards (CXS 1-1985; CXG 1-1979; CXS 118-1979)
Target Audience:
Food business operators selling prepacked food products in Singapore
Scope:
Prepacked food products sold directly to consumers in retail markets, including online platforms
Exclusions:
Loose food, food packed in the presence of the purchaser, takeaway food prepared to order, and non-retail containers for further manufacturing use
Consultation Structure:
Four parts (A–D) with nine questions and Annex I response sheet
Submission Method:
Email submission to SFA
Year:
2026
Region / City:
Global
Topic:
Food safety, allergen labelling
Document type:
Guide
Organization / Institution:
Food Standards Agency
Author:
Unknown
Target audience:
Food manufacturers, restaurant owners, consumers
Effective period:
Ongoing
Approval date:
Not specified
Amendment date:
Not specified
Year:
2025
Jurisdiction:
Wisconsin
Country:
United States
Document type:
Audit reporting requirements and reporting form
Program:
Managed Long-Term Care
Administering authority:
Department of Health Services, Division of Medicaid Services
Form number:
F-02022
Date of issue:
11/2025
Applicable entities:
Managed Care Organizations (MCOs)
Audit performer:
Independent certified public accountant (CPA) firm
Audit scope:
Claims processing for long-term care, acute, and primary services
Minimum sample size:
70 LTC claims; 85 total claims for FCP and PACE programs
Effective policy reference:
Residential services encounter reporting effective 02/01/2021
Coverage systems referenced:
ForwardHealth, DHS data warehouse
Year:
2025
Region / City:
Massachusetts
Subject:
Health Insurance, Medicaid, and CHIP
Document Type:
Implementation Guide
Organization / Institution:
MassHealth
Author:
MassHealth
Target Audience:
Healthcare providers, trading partners, and Managed Care Entities
Effective Period:
From January 1, 2012
Approval Date:
August 2025
Date of Changes:
Future updates will be included in subsequent versions
Context:
Implementation guide for electronic healthcare transactions, specifically for Medicaid and CHIP encounter data reporting under the HIPAA standards for MassHealth Managed Care Entities.
Year:
2025
Region / City:
Massachusetts
Subject:
Healthcare, Medicaid, Claims Reporting
Document Type:
Companion Guide
Organization:
MassHealth
Author:
MassHealth
Target Audience:
Healthcare providers, Trading Partners, Managed Care Entities (MCEs)
Effective Period:
From August 2025
Approval Date:
August 2025
Revision Date:
Not specified
This document is a companion guide for the ASC X12N 005010X299A1 Post-Adjudicated Claims Data Reporting:
Institutional standard, aimed at assisting MassHealth Managed Care Entities in reporting claims electronically in compliance with HIPAA.
Year:
2004
Region:
Wales
Document type:
Protocol
Organization:
NHS Wales Shared Services Partnership – Primary Care Services (NWSSP–PCS)
Target audience:
Health Boards, General Medical Practices
Subject:
Post Payment Verification, Enhanced Service Claims
Date approved:
April 2004
Relevant legislation:
Statement of Financial Entitlement (SFE), GDPR, Department of Health guidelines on patient information (DGM (96) 43)
Note:
Year
Subject:
Eviction, Small Claims
Document Type:
Legal Agreement
Target Audience:
Legal professionals, plaintiffs, defendants