№ lp_1_2_63191
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Character count: 4229
File size: 66 KB
This document outlines the procedure for the generation of labels and packaging of investigational medicinal products (IMP) in clinical trials conducted by a specific institution.
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
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Gültig ab:
04.07.2020
Note:
Author
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
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:
2024
Region / city:
Global
Theme:
Nanotechnology in food packaging
Document type:
Review article
Institution:
Not specified
Author:
Not specified
Target audience:
Researchers, food industry professionals
Period of validity:
Not specified
Approval date:
Not specified
Modification date:
Not specified
Document type:
Subcontract clauses
Subject:
Packaging and marking, data delivery, patent information, invoice review, special contract requirements
Applicable parties:
Seller, Lockheed Martin, Government
Organizations referenced:
Lockheed Martin, Missile Defense Agency
Standards and regulations referenced:
DFARS 252.211-7003, DFARS 252.227-7013, DFARS 252.227-7014, DFARS 252.227-7038, FAR 52.227-11, NISPOM DOD 5220.22-M, DoDI 5200.48, Title 49 CFR, International Maritime Dangerous Goods Code
Years referenced:
2009, 2020, 2021
Contract scope:
Purchase orders and subcontracts involving data, documentation, hardware, and research work
Intended audience:
Contractors and subcontractors performing under U.S. Government-related defense contracts
Year:
2010
Region / city:
Glendale, CO
Subject:
Pharmaceutical services, Bubble packaging
Document Type:
Sources Sought Notice
Agency:
Department of Veterans Affairs
Author:
Robert Woolfolk II
Target audience:
Service Disabled Veteran Owned Small Businesses, Veteran Owned Small Businesses, 8(a), HUBZone, and other Small Businesses
Period of validity:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Description:
The document outlines the market research announcement for a contractor to provide bubble packaging of medications for the Veterans Health Administration Salt Lake City Health Care System (VHASLCHCS).
Notifying Members:
Burundi; Kenya; Rwanda; Tanzania; Uganda
Responsible Agency:
Rwanda Standards Board (RSB)
Agency Address:
KK 15 Rd, P.O. Box 7099, Kigali, Rwanda
Contact Information:
Tel +250 788303492; Email [email protected]
Note:
; Website www.rsb.gov.rw
Notification Basis:
WTO TBT Agreement Article 2.9.2
Products Covered:
Flexible packaging materials
ICS Code:
55
Standard Reference:
DEAS 886:2025
Document Status:
Draft East African Standard
Language:
English
Number of Pages:
47
Scope:
Quantitative determination of residual solvents in flexible packaging materials by headspace gas chromatography
Exclusions:
Residues from thermal decomposition products
Applicable Materials:
Mono- or multilayer plastic films; paper; board; foil; composite materials
Objectives:
Consumer information and labelling; consumer protection; protection of human health and safety; environmental protection; quality requirements; trade facilitation
Related Documents:
ISO 5725-2
Proposed Date of Adoption:
To be determined
Proposed Entry into Force:
Six months from adoption
Final Date for Comments:
17 March 2026
Source Type:
International standards notification under WTO TBT Agreement