№ files_lp_3_process_7_090581
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Public consultation paper outlining proposed amendments to the Singapore Food Regulations on general labelling requirements for prepacked food products sold in Singapore retail markets.
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
Price: 8 / 10 USD
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Year:
2026
Region / City:
Pietermaritzburg, KwaZulu-Natal, South Africa
Subject:
Procurement of medical assistive devices
Document Type:
Tender Notice
Department:
Central Supply Chain Management, KZN Department of Health
Bid Number:
ZNB 5147/2025-H
Institutions Involved:
Various health institutions
Tender Type:
Request for Bid (RFB)
Closing Date and Time:
09 March 2026, 11:00
Briefing Meeting Date and Time:
18 February 2026, 10:00 AM
Contact Person:
Admin Enquiries: [email protected]; Technical Enquiries: [email protected]
Delivery Location:
310 Jabu Ndlovu Street, Old Boys School Building, Pietermaritzburg, 3201
Category:
Assistive devices
Sector:
Central Supply Chain Management
Document Access:
Downloadable from KZN Department of Health website at no cost
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
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:
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:
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.