Emqn Cic

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EMQN is the leading global provider of quality assurance tools and knowledge to the human molecular pathology and genetic testing community in the form of External Quality Assessment (EQA) schemes, also referred to as proficiency testing (PT). This assures the best possible clinical diagnostics test execution, accuracy, performance, interpretation, and reporting. Furthermore, EMQN’s highly qualified peer group of assessors take pride in their thought leadership position by their commitment to regularly publishing best practice guidelines. We believe that every patient should have the most accurate diagnostic test result possible. After all, many lives may depend on a correct diagnosis and appropriate treatment assessment. EMQN CIC is an incorporated Community Interest Company registered in England and Wales (Companies House Registration: 12020789). Our registered address: Third Floor, ICE Building, 3 Exchange Quay, Salford, M5 3ED

Company Details

Employees
40
Founded
-
Address
Unit 4, Enterprise House, Pencroft Way, Manchester Science Park,united Kingdom
Phone
44 (0)161 757 1591
Email
of****@****mqn.org
Industry
Hospitals And Health Care
NAICS
Health Care and Social Assistance
Social Assistance
Website
emqn.org
HQ
Manchester
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News

Microbix Assisting EMQN with Second Genetic-Test EQA Program - GlobeNewswire

Microbix Assisting EMQN with Second Genetic-Test EQA Program GlobeNewswire

EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency - Nature

EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency Nature

EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013 - Wiley Online Library

EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013 Wiley Online Library

Genetic Screening of the Usher Syndrome in Cuba - Frontiers

Genetic Screening of the Usher Syndrome in Cuba Frontiers

EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington disease - Nature

EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington disease Nature

EMQN best practice guidelines for genetic testing in dystrophinopathies - Nature

EMQN best practice guidelines for genetic testing in dystrophinopathies Nature

Spinal Muscular Atrophy in the Black South African Population: A Matter of Rearrangement? - Frontiers

Spinal Muscular Atrophy in the Black South African Population: A Matter of Rearrangement? Frontiers

Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes - Nature

Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes Nature

An Integrated Pharmacological Counselling Approach to Guide Decision-Making in the Treatment with CDK4/6 Inhibitors for Metastatic Breast Cancer - Frontiers

An Integrated Pharmacological Counselling Approach to Guide Decision-Making in the Treatment with CDK4/6 Inhibitors for Metastatic Breast Cancer Frontiers

EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta - Nature

EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta Nature

EMQN best practice guidelines for analysis and reporting of microsatellite instability in solid tumours - Nature

EMQN best practice guidelines for analysis and reporting of microsatellite instability in solid tumours Nature

One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants - Nature

One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants Nature

The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion - Nature

The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion Nature

EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome - Nature

EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome Nature

EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus - Nature

EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus Nature

Clinical Utility Gene Card for: Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP) - update 2014 - Nature

Clinical Utility Gene Card for: Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP) - update 2014 Nature

Clinical utility gene card for: Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD) - Nature

Clinical utility gene card for: Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD) Nature

Developing a Sustainable Process to Provide Quality Control Materials for Genetic Testing - Nature

Developing a Sustainable Process to Provide Quality Control Materials for Genetic Testing Nature

International genetic testing - Nature

International genetic testing Nature

Implementation of pre-emptive testing of a pharmacogenomic panel in clinical practice: Where do we stand? - British Pharmacological Society | Journals

Implementation of pre-emptive testing of a pharmacogenomic panel in clinical practice: Where do we stand? British Pharmacological Society | Journals

EMQN latest to plump for Exchange Quay space - Place North West

EMQN latest to plump for Exchange Quay space Place North West

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