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Results Entry
Results Entry
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Antibiotic Assays
Therapeutic Drug Monitoring
Blood Coagulation
Activated Clotting Time (ACT)
Activated Partial Thromboplastin Time (APTT)
Activated Protein C Resistance Assay
Antithrombin Antigen and Activity Assays
D-Dimer
Direct Oral Anticoagulant (DOAC) Assay (Pilot)
Factor II, V, VII VIII, IX, X, XI, XII Assays
Factor V Leiden/Molecular Genetics of Thrombophilia Testing
Factor XIII Screen/Assay
Fibrinogen Evaluation (Clauss method)
Haemophilia Molecular Genetics
Heparin Assay (HA)
Heparin Dosage Assessment (HDA)
Lupus Anticoagulant
Plasma Homocysteine
Plasminogen Assay
POCT D-dimer
Protein C Antigen and Activity Assay
Protein S Activity Assay
Protein S Total and Free Antigen Assay
Prothrombin Time (PT)/INR (Quick/Capillary methods)
Prothrombin Time/INR (PT for oral anticoagulant control)
PT/Diagnostic (PTD)
Quantitative Factor VIII Inhibitor
Thrombin Time (TT)
Thromboelastometry and Thromboelastography
Von Willebrand Factor Antigen: Assay
VWF:CB (collagen-binding) Assay
VWF:RCo (activity) Assay
Blood Transfusion Laboratory Practice
ABO & RhD grouping
ABO Titration
Antibody Identification
Antibody Screening
Crossmatching
Direct Antiglobulin Test (Pilot)
Fetomaternal Haemorrhage (FMH) Quantification
Fetomaternal Haemorrhage (FMH) Screening
Pretransfusion testing
Red Cell Phenotyping
Training, Assessment and Competency Tool (TACT)
Breast Cancer Screening
Breast cancer screening
Cardiac Markers
BNP
Cardiac Marker (Laboratory)
Cardiac Markers (Point of Care)
Cardiac Troponin I
Cardiac Troponin T
CKMB
Myoglobin
NT-proBNP
Cellular Pathology Technique (CPT)
Bone Marrow Trephine (BMT)
Diagnostic Non Gyn Cytology
Mohs' Procedure
Muscle Histochemistry
Neuropathology
Renal Pathology
Routine Cellular Pathology
Transmission Electron Microscopy (TEM) (Pilot)
Clinical Chemistry
Clinical Chemistry
Colorectal Cancer Screening
Erythropoietin
Faecal Haemoglobin
Faecal Markers
Faecal Pancreatic Elastase
Fructosamine
GFR Estimations (Creatinine, Cystatin C & eGFR)
Glycated Haemoglobins
Haematinics
Holotranscobalamin
Interpretative Comments
Intrinsic Factor Antibodies
Lipid Assays
Newborn Screening
Paediatric Bilirubin
Quantitative Amino Acids
Serum Indices (HIL)
Specific Proteins
Steroid Hormones
Sweat Testing
Therapeutic Drug Monitoring
Thyroglobulin
Thyroid Hormones
Tox and TDM
Urinary Catecholamines & Metabolites
Urine Chemistries
Urine Dipsticks
Vitamin Assays (Carotene, Vitamin A & E)
Vitamin B12, Folate. Ferritin, Red Cell Folate
Edinburgh Peptide Hormones
AFP, CEA and hCG
Down's syndrome scheme
FSH, LH, AMH, Prolactin and Growth Hormone
Placenta-like Growth Factor (PLGF) (Pilot)
PTH, ACTH and Calcitonin
Urinary hCG (Qualitative and Quantitative)
Genomics
Achondroplasia
Acute Lymphoblastic Leukaemia (ALL)
Additional lung cancer biomarkers (pilot)
Amniotic Fluid
Aortopathies
Bloods - Postnatal
BRCA testing in ovarian cancer (pilot)
BRCA1 & BRCA 2 Gene Screening
Breakage Syndromes (Survey)
C9orf72 related Frontotemperal Dementia and/or Amytrophic Lateral Sclerosis (C9orf72) (pilot)
Cancer Gene Panel (Pilot)
Charcot-Marie-Tooth- neuropathy type 1A & Hereditary neuropathy with liability to pressure palsies (CMT1A & HNPP)
Chorionic Villus - CVS
Circulating Tumour DNA (Pilot)
CNS Tumours (1p/19q codeletion, MGMT Promoter Methylation and IDH 1 & 2 Mutation)
Constitutional Microarray - Postnatal (in collaboration with EMQN)
Cystic Fibrosis
Dentatorubral Pallidoluysian Atrophy
DNA extraction from blood samples EQA scheme
DNA extraction from FFPE tissue samples EQA scheme
DNA extraction from fresh/frozen tissue samples EQA scheme
DNA extraction from saliva samples EQA scheme (pilot)
DNA quality measurement EQA scheme
Duchenne & Becker Muscular Dystrophies
Fabry Disease
Familial Adenomatous Polyposis
Familial Breast & Ovarian Cancer - BRCA1 & BRCA2
Familial Hypercholesterolaemia
FISH Rapid Aneuploidy
Fragile X Syndrome
Friedreich Ataxia
Genetic Counselling - Cardiovascular Genetics
Genetic Counselling - Dysmorphology (exploratory pilot)
Genetic Counselling - Monogenic Disorders (exploratory pilot)
Genetic Counselling - Oncogenetics (exploratory pilot)
Genetics - Technical Assessment Competency Tool (G-TACT)
Huntington Disease
hypertrophic Cardiomyopathy
Interpretation of pathogenicity of sequence variants
Laminopathies
Long QT Syndrome Testing
Lymphoma
Lynch Syndrome
Maternal Cell Contamination & Sexing
Mature B & T Cell Neoplasms (FISH)
Mature B & T Cell Neoplasms (G-banded Online)
Medium Chain acyl-CoA Dehydrogenase Deficiency
Microarray - acquired
Microarray - prenatal
Microsatellite Instability
Mitochondrial Diseases
Molecular Analysis in Colorectal Cancer
Molecular Analysis in Lung Cancer
Molecular Analysis in Melanoma (In collaboration with UK NEQAS for Immunocytochemistry &In-Situ Hybridisation)
Molecular Analysis of Gastro-Intestinal Stromal Tumours
Molecular Rapid Aneuploidy (In collaboration with UK NEQAS Clinical Cytogenetics)
Molecular Rapid Aneuploidy (in collaboration wtih UK NEQAS for Molecular Genetics)
Molecular Testing for Cystic Fibrosis on Blood Spots
Molecular Testing for MCADD c.985A>G Mutation on Blood Spots
Molecular Tissue Identification (pilot)
Multiple Endocrine Neoplasia Type 2
MUYTH-associated polyposis (MAP)
Myeloid Leukaemia - CML/AML/MDS
Myeloma
Myotonic Dystrophy
Neuroblastoma Tumour
Next Generation Sequencing (pilot)
Non Invasive Prenatal Testing (NIPT)
Non-Invasive Prenatal Testing for Aneuploidy (survey and exploratory pilot) (in collaboration with UK NEQAS for Molecular genetics and EMQN)
Pathogenicity of Sequence Variants
PGD Blastomere (FISH)
PGD Blastomere/Trophectoderm (Array) (pilot) (in collaboration with UK NEQAS for Molecular Genetics)
PGD Blastomere/Trophectoderm (Array/NGS) Aneuploidy Testing
PGD Blastomere/Trophectoderm (Array/NGS) Rearrangement Testing
PGD Polar Body (Array) (pilot) (in collaboration with UK NEQAS for Molecular Genetics)
PGD Sperm FISH (exploratory pilot)
POLG
Prader-Willi & Angelman Syndrome
Preimplantaion Genetic Diagnosis using Microarrays/NGS for Blastomere/Trophectoderm/Polar Body (pilot) (in Collaboration with UK NEQAS Clinical Cytogenetics)
Preimplantation Genetic Diagnosis by NGS and/or Arrays for Polar Body Testing
Preimplantation Genetic Diagnosis by NGS and/or Arrays for Trophectoderm and/or Blastomere Testing for Aneuploidies
Preimplantation Genetic Diagnosis by NGS and/or Arrays for Trophectoderm and/or Blastomere Testing for Translocations
Preimplantation Genetic Diagnosis for Mongenic Disorders
Products of Conception (POC) Array/MLPA/QF-PCR/NGS
Products of Conception/Fetal Tissue (G-banded online)
Renal/Hepato Tumour (pilot)
Report Authorisation (pilot)
Rett Syndrome
Sarcoma (In collaboration with CEQAS)
Sarcoma (pilot) (in collaboration with UK NEQAS for Molecular Genetics)
Spinal Muscular Atrophy
Spinocerebellar Ataxias
Tissue-i Online Tissue Assessment EQA Module
Von Hippel-Lindau Syndrome
Guildford Peptide Hormones
C-Peptide
Gastrin
Insulin
Insulin-like Growth Factor
Insulin-like Growth Factor Binding Protein-3
Haematology
Abnormal Haemoglobins
Automated Differential Leucocyte Count
Blood Films for Morphology, Manual Differential and Parasite Identification
Blood Parasite Screening and Identification (Haematology)
Cytochemistry: Haemosiderin staining
Digital Blood Film Morphology for CPD
DNA Diagnostics for Haemoglobinopathies
ESR
Full Blood Count
G6PD Screen and Assay
Haemoglobin only
Liquid Newborn Haemoglobinopathy Screening
Malaria Rapid Diagnostic Test (Haematology)
Manual WBC Differential Count
Newborn Sickle Screening
Nucleated red blood count (NRBC) (Pilot)
Plasma Viscosity
Reticulocyte Count
Sickle Screening only
Head & Neck Pathology
Head and Neck Pathology
Histocompatibility & Immunogenetics
Crossmatching by Flow Cytometry
Cytotoxic Crossmatching
DNA HLA Typing at 1st Field Resolution
DNA HLA Typing to 2nd or 3rd Field Resolution
Educational Cross Match
Educational Interpretive Clinical Scenarios
Educational Scheme
HFE Typing
HLA Antibody Detection
HLA Antibody Specificity Analysis
HLA Genotyping for Coeliac and other HLA associated diseases
HLA Phenotyping
HLA-B*57:01 Typing for Drug Hypersensitivity
HLA-B27 Testing
HPA Antibody Detection/Specification
HPA Genotyping
Interpretative: HFE Genotype and Hereditary Haemochromatosis
Interpretive HLA Genotype
KIR Genotyping
Immunocytochemistry & In-Situ Hybridisation
Alimentary Tract Pathology (GIST)
Alimentary Tract Pathology (Lynch Syndrome/HNPCC)
ALK IHC
Breast HER2 ISH: Interpretive and Technical
Breast Pathology (HER2 IHC)
Breast Pathology (Hormonal Receptors - Estrogen and Progesterone)
Cytopathology
Gastric HER2 IHC
General Pathology
Lymphoma Pathology
Neuropathology
Non-Small Cell Lung Cancer
Immunology, Immunochemistry & Allergy (IIA)
Acetylcholine Receptor Antibodies
Allergen Component Testing (Pilot)
Allergen Specific IgE
Alpha 1 Antitrypsin and Phenotype Identification
ANCA/GBM Antibodies
Antibodies to Nuclear and Related Antigens
Antibody to Fungal & Related Antigens
Bullous Dermatosis Antibodies
C-Reactive Protein (CRP)
C1 Esterase Inhibitor and Functional Complement Assays
Coeliac Disease Antibodies
Cryoglobulins (Image Based)
CSF Haem Pigments
CSF IgG Oligoconal Bands
CSF Proteins and Biochemistry
CSF β2 Transferrin/Beta Trace Protein
Diabetic Markers
Ganglioside Antibodies (Pilot)
General Autoimmune Serology
IgG Subclasses
Interferon Gamma Release Assays (Mycobacterium tuberculosis) IGRA TB
Monoclonal Protein Identification
Paraneoplastic Antibodies
Phospholipid Antibodies
Prostate Specific Antigen
Specific Microbial Antibodies
Total IgE
Tryptase
Tumour Markers (CA Series)
Ultrasensitive C-Reactive Protein
β2 Microglobulin
Leucocyte Immunophenotyping
Acute Myeloid Leukaemia Gene Panels (Pilot)
BCR-ABL1 and AML Translocations Identification
BCR-ABL1 Kinase Domain mutation Status (Pilot)
BRAF p.Val600Glu (V600E) Mutation Status for Hairy Cell Leukaemia (Pilot)
CD34+ Stem Cell Enumeration
FLT3 Mutation Status
IgH/TCR Clonality Status
Immune Monitoring
Immune Monitoring (Alternative Technologies)
JAK2 p.Val617Phe (V617F) Mutation Status
KIT p.Asp816Val (D816V) Mutation Status for Mast Cell Disease (Pilot)
Leukaemia Diagnostic Interpretation (Part 2)
Leukaemia Immunophenotyping (Part 1)
Low Level Leucocyte Enumeration
Major BCR-ABL1 Quantification
Minimal Residual Disease in AML
Minimal Residual Disease in B-ALL
Minimal Residual Disease in B-CLL (Pilot)
Minor BCR-ABL1 Quantification (Pilot)
NPM1 Mutation Status
Paediatric Acute Leukaemia Translocations
Paroxysmal Nocturnal Haemoglobinuria
Post-SCT Chimerism Monitoring
Microbiology
AAFB Microscopy
Anti-HBs detection
Antifungal Susceptibility
Antimicrobial Susceptibility
Blood Borne Viruses
Blood Donor Screen
C. trachomatis and N. gonorrhoeae
Clostridium Difficile
CMV DNA Quantification
Community Medicine
Cryptococcal antigen detection
Diagnostic Serology: hepatitis screen
EBV DNA Quantification
Faecal Pathogens
Fungal Biomarkers
General Bacteriology
Genital pathogens
HBV DNA Quantification
Hepatitis B Serology
Hepatitis C RNA Detection
Hepatitis C Serology
Hepatitis E serology
HIV 1 RNA Quantification
HIV Point of Care
HIV Serology
Immunity Screen
Measles and Mumps IgG Serology
Molecular Detection Mycobacteria
Molecular detection of HEV RNA
Molecular Detection of HPV
Molecular Detection of Respiratory Viruses
Molecular Detection of Viruses in CSF
MRSA Screening
Mycobacteria Culture
Mycology
Parvovirus B19 and Rubella Serology
Respiratory Rapid: RSV
Rubella IgG Serology
Syphilis Serology
Urinary Antigens
Viral Gastroenteritis
Virus identification
Neuropathology
Neuropathology
Parasitology
Blood Parasitology
Faecal Parasitology
Malaria Rapid
Molecular Diagnosis of Malaria
Parasite Serology
Toxoplasma Serology
Reproductive Science
Andrology: Semen Analysis (Sperm Motility, Concentration & Morphology)
Embryology: Embryo Morphology
Trace Elements
Aluminium in Water/Dialysis Fluid
Copper and Iron in Solid Martices e.g. Liver
Lead, Cadmium, Manganese, Arsenic, Magnesium, Mercury, Zinc, Selenium, Thallium, Chromium and Cobalt in Blood
Mercury, Cadmium, Copper, Iron, Zinc, Chromium, Cobalt, Arsenic, Lead, Manganese, Nickel, Thallium and Selenium in Urine
Zinc, Copper, Aluminium, Selenium, Chromium and Cobalt in Serum
Vitamin K
Mk-4 at endogenous conecentrations in human serum
MK-7 at endogenous concentrations in human serum
Vitamin K1 at endogenous concentrations in human serum
Vitamin K1, 2, 3-epoxide at endogenous concentrations in human serum
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