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Reference Laboratory Genetics

  • Reference Laboratory Genetics
  • Calle Pablo Iglesias 57
  • 08908 L'HOSPITALET DE LLOBREGAT
  • SPAIN
  • Status : Private for-profit
  • Phone : 34 932593700
  • Additional Phone : -
  • Fax : -
  • Website
  • Contact
  • EUGT number : EUGTES410947

Contacts

Quality management

Accreditation
 Accreditation

Accreditation
Organism
Year
Accreditation scope

EQA
 EQA

EQA scheme(s) organized by CEQAS

Rapid aneuploidy FISH
2015, 2016, 2017

EQA scheme(s) organized by EMQN

11p-Imprinting Disorder Scheme (BWS/SRS)
2018, 2019
ADPKD (Adult dominant polycystic kidney disease)
2018, 2019
AZF (Y-Chromosome microdeletions)
2015, 2016, 2017, 2018, 2019
CAH (Congenital Adrenal Hyperplasia)
2015, 2016, 2017, 2018, 2019
Cardiac genetics - arrthymias
2019
DFNB1 (Hereditary Deafness)
2019
DM (Myotonic dystrophy)
2015, 2016, 2017, 2018, 2019
DMD (Duchenne and Becker muscular dystrophies)
2015, 2016, 2017, 2018
FH (Familial hypercholesterolemia - pilot scheme)
2019
FRAX (Fragile X syndrome) - full scheme
2015, 2016, 2017, 2018, 2019
Germline NGS mutation testing
2016, 2017, 2018, 2019
HBOC (Hereditary Breast and Ovarian Cancer testing)
2015, 2016, 2017, 2018, 2019
HD (Huntington disease)
2015, 2016, 2017, 2018, 2019
HNPCC (Hereditary non-polyposis colon cancer)
2019
MEN2 (Multiple Endocrine Neoplasia Type 2)
2015, 2016, 2017
Mitochondrial metabolic disorders
2018, 2019
Non-invasive prenatal testing (NIPT) for common aneuploidies
2017, 2018
Non-invasive prenatal testing (NIPT) for fetal sexing
2017, 2018
OI (Osteogenesis imperfecta)
2017
PWAS (Prader-Willi and Angelman syndromes)
2015, 2016, 2017, 2018, 2019
RB (Retinoblastoma)
2019
SEQ (DNA sequencing) - Full scheme
2016, 2017, 2018, 2019
WIL (Wilson disease)
2015
aCGH/ Microarrays
2015, 2016, 2017, 2018, 2019
ccfDNA (Cell free fetal DNA for sex determination)
2015, 2016

EQA scheme(s) organized by GenQA

Amniotic fluid
2019, 2020
Ataxia and spastic paraplegia
2020, 2021
Cardiac Disorders
2020, 2021
Chorionic Villus
2019, 2020
Clinical Genetics - Cardiovascular Disorders
2021
Cystic Fibrosis (CF) and CFTR-related disorders
2020, 2021
Dementia/ALS
2019
Disorders of Sex Development (DSD)
2020
Epilepsy disorders
2020, 2021
Familial Colorectal Cancer and Polyposis
2020, 2021
Familial endocrine tumour predisposition disorders
2020, 2021
Gastrohepatology disorders
2021
Hereditary Breast and Ovarian Cancer (HBOC) disorders
2020
Hypotonic Infant
2020
Imprinting disorders
2020, 2021
Inborn Errors of Metabolism
2021
Mitochondrial disease
2020, 2021
Muscular Dystrophies
2020, 2021
Myeloid Disorders
2020, 2021
Neurodegenerative Disorders
2020, 2021
Neurofibromatosis and Rasopathies
2020, 2021
Pathogenicity of germline sequence variants (Classification & Interpretation)
2019, 2020, 2021
Prenatal constitutional Copy Number Variant (CNV) detection
2019, 2020, 2021
Prenatal karyotyping
2021
Rapid Prenatal Aneuploidy FISH
2018
Renal Disorders
2020, 2021
Skeletal dysplasia
2020, 2021
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.