№ lp_2_1_22878
File format: docx
Character count: 38165
File size: 96 KB
Trust policy establishing mandatory standards for the requesting, identification, labelling, acceptance, and rejection of biological specimens submitted to LTHT Pathology, including requirements for high-risk infectious samples.
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
Price: 8 / 10 USD
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Year:
2018
Region / City:
Jaipur, Rajasthan, India
Document Type:
Tender Notice
Organization:
The LNM Institute of Information Technology, Jaipur
Contact:
Finance & Purchase Officer, Phone: 0141 5191733, Email: [email protected]
Scope:
Supply of spares and maintenance of 2x1000 kVA transformers, LT & HT panels, ACBs, VCBs, and capacitor panels
Eligibility:
Completion of at least five similar projects
Submission Deadline:
27 June 2018
Location of Work:
Gram-Rupa Ki Nangal, Post-Sumel, Via-Jamdoli, Jaipur
Technical Requirements:
Detailed inspection, cleaning, testing, and repair of transformers, ACBs, VCBs, panels, and related equipment
Financial Requirements:
Price bid including all taxes, transportation, manpower, lodging, and boarding
Year:
2020
Region / City:
Leeds, UK
Subject:
Hematology / G6PD Testing
Document Type:
Laboratory Referral Form
Institution:
Centre for Laboratory Medicine, SJUH
Author:
Blood Sciences Department
Intended Audience:
Healthcare professionals submitting patient samples
Specimen Requirements:
1 x Fresh EDTA patient sample (3ml minimum) and 1 x anonymised EDTA travel control (1ml minimum)
Parameters Measured:
Hb, WBC, Reticulocytes, MCH, RBC, Platelets
Guidelines Compliance:
BSH Guidelines 2020
Form Version:
Qpulse Code BSHC-FOR-178 v 1.2
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
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
Version:
1.5.0.0
Protocol Posting Date:
June 2024
CAP Laboratory Accreditation Program Protocol Required Use Date:
March 2025
Authors:
Gulisa Turashvili, MD, PhD; Uma G. Krishnamurti, MD, PhD; Barbara A. Crothers, DO; Giovanna A. Giannico, MD; Krisztina Hanley, MD; Anna Plotkin, MD; Anthony N. Karnezis, MD, PhD.
Note:
Accreditation Requirements
Date of Protocol Posting:
June 2024
Date of Required Use:
March 2025
Year:
2010
Region / City:
Grahamstown
Subject:
Biomaterials transfer, research agreements
Document Type:
Agreement
Organization / Institution:
South African Institute for Aquatic Biodiversity (SAIAB)
Author:
SAIAB Collections Manager
Target Audience:
Researchers, research institutions
Effective Period:
Not specified
Approval Date:
18 March 2010
Modification Date:
Not specified
Context:
Legal agreement for the transfer of biomaterials from SAIAB collections to researchers for research purposes.
Year:
2026
Region / City:
Alberta, Canada
Theme:
Paleontology, Dinosaur Anatomy
Document Type:
Research Article
Institution:
University of Calgary, Royal Tyrrell Museum of Palaeontology
Author:
Jared T. Voris, Darla K. Zelenitsky, François Therrien, Ryan C. Ridgely, Philip J. Currie, Lawrence M. Witmer
Target Audience:
Paleontologists, Researchers in Evolutionary Biology
Period of Activity:
Cretaceous Period
Approval Date:
2026
Date of Revisions:
None specified