Each request accepted by the laboratory for examination(s) shall be considered an agreement. For further details including a summary of the departments obligations and assurances to service users see NHSGGC Pathology Department Terms of Service.
If you are sending a sample to us for testing from outside NHSGGC, please contact the department for details on the costing of tests.
All specimens must be accompanied by an appropriately completed Trakcare form, or if this is not possible a NHSGGC Pathology request form (available through PECOS – product code 100509) may be used. If appropriate, an accompanying speciality request form (placenta, HPV cytology, muscle etc.) should also be included.
Level 3, Laboratory Medicine and Facilities Management Building
Queen Elizabeth University Hospital
Tel: 0141 354 9513 (89513) or 0141 354 9514 (89514)
Please use a purple bag for histopathology specimens and a white bag for cervical cytology specimens
Minimum Sample Acceptance Criteria
CHI/Unique identifier, Surname & Forename or if no CHI/unique identifier, the Surname, Forename and Date of Birth must be provided.
A minimum of 3 matching patient identifiers across both the specimen pot labels and forms are required to accept a specimen and meet legislative requirements.
Only Specimen containers and Forms that satisfy the essential criteria listed below can be accepted into the department.
Request Form
Essential:-
CHI Number or a temporary unique identifier (e.g. ZP number)
Patient’s Full Name or unique coded identifier
Date of Birth
Nature of Specimen including qualifying details (Any Danger of Infection information is essential)
Desirable:-
Patient’s Address including Postcode (essential if no CHI number)
Clinical Information/history including risk/danger of infection (essential for fresh tissue and frozen section)
Date and time of sampling
Practitioner’s contact number (bleep or extension)
Gender
Location and destination of report
Requesting Practitioner
Investigation Required
Sample Container
Essential:-
CHI number or a temporary unique identifier (e.g. ZP number)
Patient’s Full name or unique coded identifier
Date of Birth
Nature of Specimen or identifier including qualifying details
Labelling to indicate if there is a risk/danger of infection
Desirable:-
Date and Time of Sampling
Other Essential Information
The full address to which the report should be sent must also be included.
N.B: Pre-printed labels do not indicate the address to which the report should be sent.
A short clinical history must also be provided.
A brief clinical history is invaluable in the interpretation of the histological findings and should be given in every case.
As many pathology cases require considerable clinico-pathological discussion before a diagnosis can be reached, it is essential that the name of the patient’s consultant, the name of the requesting doctor and the contact telephone or page numbers are put on the request form where asked.
If the report is required urgently this should be stated on the request form along with a contact telephone number or page number.
The laboratory cannot supply a report on unlabelled specimens or specimens received without request forms.
Failure to provide the required information may result in delays in processing specimens and/or in the provision of a Pathology report to the appropriate location.
Fixation (Tissue Preservation)
Normally, specimens should be transferred in a sealed container with 10% neutral buffered formalin, which prevents tissue decay, ideally the volume of formalin should be at least 10 times the volume of the specimen, but for major resections this may not be possible. Please ensure that containers are properly sealed before dispatch as leaking specimens will not be picked up by Transport/ Facilities staff. If you have a Formalin spill, follow your own spill procedures.
No fixative should be added if:
a frozen section is requested (including: brain biopsies taken mid surgery for smear analysis, muscle biopsies and paediatric rectal biopsies – see individual sections for more information)
the specimen is thought to be a lymphoma – whole lymph nodes only
there is a need to collect and process fresh surplus tissue for medical research purposes
The sample is for Immunofluorescence
Sending Fresh Tissue
All fresh tissue must be delivered to the Pathology Department immediately and Pathology Specimen Reception should be notified that fresh tissue has been sent.
Tel: 0141 354 9513 (89513) or 0141 354 9514 (89514)
If you are unsure of the correct procedure, contact Pathology Specimen Reception for advice on the telephone numbers above.
Delay in receipt of a “fresh” specimen may make diagnosis impossible.
Fixatives and specimen jars are available from:
Specimen Reception (L3/B/021),
NHSGGC Pathology Department
Level 3, Laboratory Medicine and Facilities Management Building
Queen Elizabeth University Hospital
Tel: 0141 354 9513 (89513) or 0141 354 9514 (89514)
Urgent Specimens for Pathology
Requests for urgent results should be clearly marked on the request form and contact telephone or page number provided.
The consultant pathologist should be notified before the specimen is sent if an urgent result is required.
It is the responsibility of the clinical team to ensure that emergency/urgent specimens are transported urgently to the Pathology Laboratory.
Precautions for “Danger of Infection” (DOI)
In practice, these are specimens that carry the risk of transmitting Hepatitis B virus, Hepatitis C virus, HIV, M. tuberculosis and other category III pathogens.
The Clinical Microbiology Department should be contacted where there is any uncertainty.
Such specimens, include those from confirmed or suspected cases of the disease, known carriers (e.g. those known to be hepatitis antibody or antigen positive), as well as patients from an ‘at risk’ group (e.g. drug abusers).
‘Danger of infection’ (DOI) stickers must be put on the specimen bag, the request form and the specimen container.
If the nature of the DOI is known please include this in the clinical details.
Specimen bags should be sealed so that they can be opened without the use of sharp or pointed instruments.
For large specimens, containers should be enclosed in individual plastic sacks tied at the neck. The request form should be placed in a plastic envelope which is then securely tied to the neck of the sack.
“Danger of Infection” specimens should always be sent in an adequate volume of buffered formalin.
Pathology Non-Conformances (Unable to Accept Specimen)
If a specimen is received in Pathology and the specimen and/or request form has been mislabelled, is unlabelled or there are discrepancies between the request form and specimen container, the Laboratory staff will make every attempt to contact the sender to clarify the error, including telephoning the source and contacting requesting clinician etc. identified from any information that has been supplied.
If the Laboratory staff are unable to rectify the problem by telephone, a “Non-conformance letter” will be sent to the requesting clinician.
This letter is accompanied by the request form and identifies the nature of the non-conformance with a request that this is rectified, and the requesting clinician takes responsibility for the changes.
Specimens will not be returned but will be kept in Pathology Specimen Reception labelled with the appropriate non-conformance number, until the non-conformance has been resolved.
Cytology Non-Conformances
The laboratory cannot supply a report on unlabelled specimens or specimens received without request forms. Failure to provide the required information may result in delays in processing specimens and/or in the provision of a pathology report to the appropriate location.
In the event of an urgent specimen being received in diagnostic cytology, where the specimen and/or request form has been mislabelled, the technical staff in the lab will make every attempt to contact the sender and clarify the mislabelling error, including telephoning the source and contacting the requesting clinician etc. identified from any information that has been supplied.
In the event of there being insufficient information to allow cytology to contact the sender, the specimen will be kept refrigerated for one week, in the hope that the lab will be contacted. If no contact has been made at the end of this period, the specimen will be discarded.
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The NHSGGC Pathology Department provides a comprehensive diagnostic Histopathology, Cytopathology and Mortuary service for adults and children in the Greater Glasgow and Clyde area, including the laboratory part of the cervical screening programme for NHSGGC, Grampian, Tayside, Orkney, Shetland, Ayrshire and Arran. In addition, the department supports a number of specialist services, wider managed clinical networks, regional and supra regional services examples of which include Gynaecological, Ophthalmic, Osteoarticular services, West of Scotland Heart and Lung Centre, Neuropathology and Paediatric Pathology. Mortuary services are additionally provided for the Crown Office Procurator Fiscal (COPFS) and Police Scotland.
Important Notice: Extended Turnaround Times
The Pathology Department are currently experiencing longer than usual turnaround times due to a backlog in reporting. Our team is working diligently to address this issue and it has been escalated via all appropriate governance channels
Departmental Links
Please use the links below to access specific information for each of our laboratory areas:
The NHSGGC Pathology Department is located at the Queen Elizabeth University Hospital (QEUH) on the 3rd floor of the Laboratory Medicine and Facilities Management Building.
Laboratory Opening Hours
The Pathology Department is open:
Monday to Friday: 9:00am – 5:00pm
Saturday and Public Holidays: 8:00am – 12:00pm
The Pathology Department specimen reception is also open Monday to Friday from 5:00pm – 7:00pm for the receipt and handling of specimens delivered by “late vans” and couriers.
Pathology Contact Details
NHSGGC Pathology Department
Laboratory Medicine and Facilities Management Building (Level 3)
Queen Elizabeth University Hospital
1345 Govan Road
Glasgow
G51 4TF
Scotland
UK
For General Enquiries:
Tel: 0141 354 9500 (89487) Option 6
For Results:
Tel: 0141 354 9476 (89487) Option 2
For Technical Enquiries/Sending Specimens:
Tel: 0141 354 9513 (89513)/0141 354 9514 (89514)
For Mortuary Enquiries:
Tel: 0141 354 9357 (89357)
Accreditation
The NHSGGC Pathology department has been accredited by the United Kingdom Accreditation Service (UKAS), using the ISO 15189:2022 set of international laboratory standards. This assessment provides formal recognition of our ability to provide a high-quality laboratory and clinical service across all our diagnostic specialities (Histology, Neuropathology, Diagnostic Cytology, Andrology, HPV Screening, Electron Microscopy, Post-mortem and Mortuary Services).
Where possible the department participates in national external quality assurance schemes for all testing procedures/medical reporting specialties. Where established EQA schemes are not available inter laboratory comparison or alternative external quality assurance schemes have been set up.
The full list of accredited tests provided by the department can be seen in our schedule of accreditation.
UKAS GEN 6
The Pathology department utilises the Telepath Laboratory Information Management System (LIMS). Due to the limitations of this software, we are currently unable to fully meet the requirements of the UKAS publication GEN 6 – Reference to accreditation and multilateral recognition signatory status.
This publication sets out the requirements of reports/results released by the laboratory containing the appropriate use of UKAS logos and identifying any tests that are accredited and those that are not. The LIMS currently being utilised within Pathology does not allow us to present the UKAS logo within our reports. Whilst it is possible to enter a small amount of additional text without any difference in formatting at the end of each report, the referencing to the accreditation of tests could potentially interfere or cause the misinterpretation of pathology results (particularly with molecular and companion diagnostic tests such as PD-L1 that already have statements at the end of the reports explaining treatment/scoring decisions and the specific criteria required to be met). Where possible the department is including a small statement at the end of reports if a test used is out of our scope of accreditation.
The Pathology department have risk assessed this. Although we are not able to present this information on our reports the department’s user manual and website present full details of our accreditation, including a link to the UKAS page for our up to date schedule of accreditation and a list of currently out of scope techniques including details of progress made to add them to our scope or reasons for them currently being unaccredited.
A number of investigation techniques carried out by the department are currently outside the scope of accreditation (see table below). This will usually be due to the technique not being performed frequently or being controlled/run by another department. However, the department will complete internal validation and IQC procedures before the implementation of any technique and participate in national external quality assurance (EQA) schemes or alternatives where possible:
NHSGGC Pathology Department Out of Scope Techniques
Test/Investigation
Internal Validation and IQC
EQA Scheme Participation
UKAS Extension to Scope Status
Joint Fluid/Crystal Analysis
Yes
Signed up to Pilot
Not in Scope
Mohs clinic (run by Dermatology)
Yes
Not in Scope
Appearance and Viscosity for Andrology testing
Yes
Not for these criteria
Not UKAS accredited parameters
Digital Pathology
Yes
Signed up to Pilot
Expected 2026
E17 (ICC)
Not acquired yet
Expected 2026
SF1 (ICC)
Not acquired yet
Expected 2026
Hologic Genius Digital Diagnostics System (Cytology)
In Progress
Expected 2027
Research Use Only Antibodies – Immunocytochemistry (ICC)
A number of the antibody markers in the department’s immunocytochemistry repertoire are designed for research use only. These antibody markers undergo stringent and strict verification testing before diagnostic use and performance is closely monitored via internal and external quality control measures. Here is a list of the research use only antibodies currently in use:
AMH
Amyloid P
a-Syn
ATRX
B-Amyloid (BA4)
BAP-1
BAPP
BetaF1
BOB1
C4D
C5B-9
CA19.9
CD15
CD35
CD42b
CD43 (MT1)
CD45-RO
CD303
CEA (MONO)*
CK3
CK10
CK12
Claudin 4
CMYC
CXCL13
DNAJB9
EBNA-2
GLP-1
Glucagon
GLUT-1
H3K27M
G-34 (Histone H3.3 M)
H B Core Ag
H B Surface Ag
HPV
HSV-1
LAM A2
LAM A5
LAM B1
LAM B2
Neomysin
IgG4
INI-1
K36 (Histone H3M)
LEF-1
MAC-387
MGMT
MTAP
MUC4
NEUN
NF (Neurofilament)
NUT1
P16
P21 (WAF)*
P24
Parvovirus
PAX8
PD1
PHOX2B
Pituitary – ACTH
Pituitary – LH
Pituitary – Prolactin
PLA2R1
SDHB
Serotonin 5HT
SMARCA4
STAT6
Surfactant Apolipoprotein (SP-A)
SV40
TAU
TCR-Delta
Tenascin
Toxoplasma
Villin*
VIP (Vasoctinpolypep)
Ubiquitin
* = a new CE marked (non-research use only) version of this antibody marker is in the progress of being verified for diagnostic use.
For further information on these research use only antibody markers or the departments immunocytochemical (ICC) repertoire, please contact the ICC laboratory (0141 354 9518) or The Advanced Staining Specialty Manager (0141 354 9528).
See User Manual for full list of Speciality Pathologists teams.
User Feedback, Complaints and Compliments
The department aims to provide a first-class service. If we have failed to meet your expectations, please do not hesitate to contact us, henceforth we can attempt to rectify the situation.
If you wish to discuss a report, please telephone the consultant whose name appears at the bottom of the report, in the first instance. The consultant will be happy to review the case and seek a further opinion within or out with the department as required.
User Feedback Survey
We invite all our users to complete our user survey form. Please return via email to the Compliance and Transformation Manager. The information obtained from this survey will allow us to develop and improve the service we offer. We greatly appreciate the time and effort taken to complete this.
General Comments, Complaints and Feedback
For general complaints/compliments/comments on the service please contact:
Clinical Biochemistry is the division of Laboratory Medicine that deals with the measurement of chemicals in blood, urine and other body fluids. These test results are used for the diagnosis and management of the disease. The Clinical Biochemistry services provide advice to Clinicians on the appropriate use of tests, interpretation of results and follow up investigations that may be required.
Scottish Trace Element & Micronutrient Diagnostic & Research Laboratory
The Scottish Trace Element and Micronutrient Diagnostic and Research Laboratory (STEMDRL) is in part centrally funded by the National Services Division of NHS Scotland to provide a specialist analytical and advisory service for trace elements and vitamins.
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