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Nzoz genomed > Certificates

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Our certificates    

Genomed obtained the highest scores in the European Molecular Quality Network external assessment scheme in DNA Sequencing - Sanger (Full version) and Next Generation Sequencing for the year 2018. The highest scores have been also obtained in pilot EQAs covering testing for germline and somatic variants in Ovarian Cancer for targeted therapy qualification (Ovarian cancer vGermline, Ovarian cancer vSomatic).

NZOZ Genomed obtained the highest scores in the 2018 External Quality Assessment Scheme for Cystic Fibrosis (Cystic Fibrosis Network) in the field of:
  • genotyping, data interpretation and reporting for cystic fibrosis and CFTR-dependent diseases


The Genomed diagnostic laboratory obtained certificates of the Polish Society of Human Genetics: "Laboratory recommended by the Polish Society of Human Genetics" for the years 2017-2019 in the field of genetic testing (molecular techniques).




The diagnostic laboratory is on the list of laboratories that is kept by the National Chamber of Laboratory Diagnosticians at number 2854.

The Genomed diagnostic laboratory obtained certificates of the Polish Society of Human Genetics: „Laboratory recommended by the Polish Society of Human Genetics” for the years 2015-2016 in the field of genetic testing (molecular techniques).



NZOZ Genomed obtained the highest scores in the 2016 External Quality Assessment Scheme for Cystic Fibrosis (Cystic Fibrosis Network) in the field of:
  • genotyping, data interpretation and reporting for cystic fibrosis and CFTR-dependent diseases


NZOZ Genomed successfully participated in the 2015 External Quality Assessment Scheme for Cystic Fibrosis (Cystic Fibrosis Network) in the field of:
  • genotyping, data interpretation and reporting for cystic fibrosis and CFTR-dependent diseases



Genomed SA obtained the highest scores in the European Molecular Quality Network 2017 external assessment schemes in the field of genotyping, interpretation and reporting of results for Congenital Adrenal Hyperplasia (CAH), mitochondrial DNA defects (mtDNA), non-invasive prenatal testing (NIPT (Aneuploidies – pilot)) and NextGen DNA Sequencing of somatic variants (vSomatic)), osteogenesis imperfecta (OI), and spinal muscular atrophy (SMA).


Genomed obtained highest scores in the European Molecular Quality Network external assessment schemes in the field of DNA sequencing (DNA-Seq, Full Scheme), Familial autosomal dominant hypercholesterolemia (FHL) and Fragile X Syndrome (FRAX, Full scheme) for the year 2016.

Genomed obtained the highest scores in the European Molecular Quality Network external assessment schemes in the field of Next-Generation Sequencing) (NGS) for the year 2015

Genomed obtained the highest scores in the European Molecular Quality Network 2015 external assessment schemes in the field of genotyping, interpretation and reporting of results for nonsyndromic hearing loss and deafness (DFNB1), multiple endocrine neoplasia type 2 (MEN2) and familial adenomatous polyposis (FAP).

Genomed obtained the highest scores in the European Molecular Quality Networkexternal assessment schemes in the field of genotyping for the year 2014  for DNA-SEQ (Full), Lung Cancer (NSCLC) and NextGen Sequencing (NGS) Schemes.

Genomed obtained the highest scores in the European Molecular Quality
Network
external assessment schemes in the field of genotyping
and interpretation of results for Familial Breast Cancer (Full Scheme)
and  Congenital Adrenal Hyperplasia
for the year 2014.



NZOZ Genomed obtained certificates of EMQN ( European Molecular Quality Network ) in the field of genotyping assessment and interpretation for
  • Identification of AZF microdeletion of the Y chromosome in male infertility
  • Haemochromatosis
  • BRCA1 and BRCA2
  • Detection of any mutations (Mutation Scanning)
  • Sequencing


NZOZ Genomed obtained certificates of EMQN ( European Molecular Quality Network ) in the field of genotyping assessment and interpretation for
  • Y-Chromosome microdeletions
  • Fragile X syndrome testing (PCR ONLY)
  • Spinal Muscular Atrophy



NZOZ Genomed obtained the certificate of CF Network ( Cystic Fibrosis Network ) in the field of

  • genotyping and data interpretation for cystic fibrosis and CFTR-dependent diseases



The Genomed diagnostic laboratory belongs to the Network of Reference Laboratories of the Polish Society of Human Genetics



NZOZ Genomed obtained the certificate of the Network of Reference Laboratories of the Polish Society of Human Genetics in the field of diagnostics of
  • Premature Ovarian Failure
  • Spinal muscular atrophy
  • MTHFR Deficiency
  • Noonan Syndrome
  • Fragile X Syndrome
  • Angelman and Prader-Wilii syndrome
  • Niemann-Pick disease, type C


NZOZ Genomed obtained the certificate of the Network of Reference Laboratories of the Polish Society of Human Genetics in the field of diagnostics of
  • Alpha1-antitrypsin deficiency
  • Lactase persistence, adult type, hypolactasia
  • Pancreatitis (acute and chronic)
  • Cystic fibrosis
  • Familial Hipercholesterolemia
  • Cardiomiopathy hypertrophic
  • Hyperprothrombinaemia
  • Glaucoma juvenile open angle
  • Age-related macular degeneration
  • Mucopolysaccharidosis type VI


NZOZ Genomed obtained the certificate of the Network of Reference Laboratories of the Polish Society of Human Genetics in the field of diagnostics of
  • Familial haemochromatosis


NZOZ Genomed obtained the certificate of the Network of Reference Laboratories of the Polish Society of Human Genetics in the field of diagnostics of
  • Recurrent pregnancy loss
  • Male infertility (analysis of mutations in the CFTR gene and identification of a microdeletion of the AZF region in chromosome Y
  • Androgen insensitivity syndrome



NZOZ GENOMED took part in the newborn screening quality assurance program (cystic fibrosis mutation detection survey) organised by CDC/APHL (US). Our laboratory obtained 100% satisfactory results.



 
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