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Country
PT provider
PT scheme
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437654 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Cerebrospinal Fluid Cytology Course (only in German) [Liquor-Zytodiagnostik - Ringversuch vor Ort] Cerebrospinal Fluid Cytology Course (only in German) [Liquor-Zytodiagnostik - Ringversuch vor Ort] 2019-03-12
PT provider ID (119881)

159540 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Virus Genome Detection – Hepatitis B Virus Genotyping [Virusgenom-Nachweis – Hepatitis-B-Virus Genotypisierung] Virus Genome Detection – Hepatitis B Virus Genotyping [Virusgenom-Nachweis – Hepatitis-B-Virus Genotypisierung] 2019-03-12
PT provider ID (119881)

159552 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Virus Genome Detection – Hepatitis A Virus [Virusgenom-Nachweis – Hepatitis-A-Virus] Virus Genome Detection – Hepatitis A Virus [Virusgenom-Nachweis – Hepatitis-A-Virus] 2019-03-12
PT provider ID (119881)

159548 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Virus Genome Detection – Parvovirus B19 [Virusgenom-Nachweis – Parvovirus B19] Virus Genome Detection – Parvovirus B19 [Virusgenom-Nachweis – Parvovirus B19] 2019-03-12
PT provider ID (119881)

423020 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Engraftment- and Chimerism Diagnostics (618) [Engraftment- und Chimärismusdiagnostik (618)] Engraftment- and Chimerism Diagnostics (618) [Engraftment- und Chimärismusdiagnostik (618)] 2023-10-23
PT provider ID (119881)

1083971 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 44 – C-C motif chemokine receptor 5 (764) [Molekulargenetik 44 - C-C Motif Chemokine Receptor 5 (764)] Molecular Genetics 44 – C-C motif chemokine receptor 5 (764) [Molekulargenetik 44 - C-C Motif Chemokine Receptor 5 (764)] 2023-10-23
PT provider ID (119881)

1083966 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 43 – Angiotensin Converting Enzym Apolipoprotein (763) [Molekulargenetik 43 - Angiotensin Converting Enzym (763)] Molecular Genetics 43 – Angiotensin Converting Enzym Apolipoprotein (763) [Molekulargenetik 43 - Angiotensin Converting Enzym (763)] 2023-10-23
PT provider ID (119881)

1083955 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 42 – Dihydropyrimidin Dehydrogenase (762) [Molekulargenetik 42 - Dihydropyrimidin Dehydrogenase (762)] Molecular Genetics 42 – Dihydropyrimidin Dehydrogenase (762) [Molekulargenetik 42 - Dihydropyrimidin Dehydrogenase (762)] 2023-10-23
PT provider ID (119881)

159241 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 41 – Spinal Muscular Atrophy (SMN1 und SMN2 genes) (787) [Molekulargenetik 41 - Spinale Muskelatrophie (SMN1 und SMN2 Gene) (787)] Molecular Genetics 41 – Spinal Muscular Atrophy (SMN1 und SMN2 genes) (787) [Molekulargenetik 41 - Spinale Muskelatrophie (SMN1 und SMN2 Gene) (787)] 2023-10-23
PT provider ID (119881)

159221 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 39 – mlH1 MSH2 MSH6 PMS2 (HNPCC) (783) [Molekulargenetik 39 - MLH1 MSH2 MSH6 PMS2 (HNPCC) (783)] Molecular Genetics 39 – mlH1 MSH2 MSH6 PMS2 (HNPCC) (783) [Molekulargenetik 39 - MLH1 MSH2 MSH6 PMS2 (HNPCC) (783)] 2023-10-23
PT provider ID (119881)

425247 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 38 – Lactase-gene -13910T>C (MCMG Gen, IVS13 C-T, rs9988235, hgVS: C.1917+326 C>T) (770) [Molekulargenetik 38 - Laktase-Gen -13910T>C (MCMG Gen, IVS13 C-T, rs9988235, hgVS: C.1917+326 C>T) (770)] Molecular Genetics 38 – Lactase-gene -13910T>C (MCMG Gen, IVS13 C-T, rs9988235, hgVS: C.1917+326 C>T) (770) [Molekulargenetik 38 - Laktase-Gen -13910T>C (MCMG Gen, IVS13 C-T, rs9988235, hgVS: C.1917+326 C>T) (770)] 2023-10-23
PT provider ID (119881)

159141 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 37 – K-ras Codon 12/13/61 (776) [Molekulargenetik 37 - K-ras Codon 12/13/61 (776)] Molecular Genetics 37 – K-ras Codon 12/13/61 (776) [Molekulargenetik 37 - K-ras Codon 12/13/61 (776)] 2023-10-23
PT provider ID (119881)

159228 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 36 – Huntingtin Disease (HTT Gene, Ag Repeats) (784) [Molekulargenetik 36 - Huntingtin Krankheit (HTT Gen, Ag-Repeats) (784)] Molecular Genetics 36 – Huntingtin Disease (HTT Gene, Ag Repeats) (784) [Molekulargenetik 36 - Huntingtin Krankheit (HTT Gen, Ag-Repeats) (784)] 2023-10-23
PT provider ID (119881)

159217 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 34 – Connexin 26 (gJB2 gene, 35 del g) (782) [Molekulargenetik 34 - Connexin 26 (gJB2 Gen, 35 del g) (782)] Molecular Genetics 34 – Connexin 26 (gJB2 gene, 35 del g) (782) [Molekulargenetik 34 - Connexin 26 (gJB2 Gen, 35 del g) (782)] 2023-10-23
PT provider ID (119881)

159207 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 33 – Fragile X Syndrome (FMR1 Gene, CGG Repeats) (781) [Molekulargenetik 33 - Fragiles-X-Syndrom (FMR1 Gen, CGG-Repeats) (781)] Molecular Genetics 33 – Fragile X Syndrome (FMR1 Gene, CGG Repeats) (781) [Molekulargenetik 33 - Fragiles-X-Syndrom (FMR1 Gen, CGG-Repeats) (781)] 2023-10-23
PT provider ID (119881)

159202 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 32 – Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) (DMD Gene) (780) [Molekulargenetik 32 - Muskeldystrophie Typ Duchenne (DMD) und Becker (BMD) (DMD-Gen) (780)] Molecular Genetics 32 – Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) (DMD Gene) (780) [Molekulargenetik 32 - Muskeldystrophie Typ Duchenne (DMD) und Becker (BMD) (DMD-Gen) (780)] 2023-10-23
PT provider ID (119881)

159149 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 31 – CYP2D6 DPD IL28B (777) [Molekulargenetik 31 - CYP2D6 DPD IL28B (777)] Molecular Genetics 31 – CYP2D6 DPD IL28B (777) [Molekulargenetik 31 - CYP2D6 DPD IL28B (777)] 2023-10-23
PT provider ID (119881)

159125 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 30 – CYP2C9 CYP2C19 VKORC1 TPMT (775) [Molekulargenetik 30 - CYP2C9 CYP2C19 VKORC1 TPMT (775)] Molecular Genetics 30 – CYP2C9 CYP2C19 VKORC1 TPMT (775) [Molekulargenetik 30 - CYP2C9 CYP2C19 VKORC1 TPMT (775)] 2023-10-23
PT provider ID (119881)

159101 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 29 – Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency (CYP21A2 Gene) (773) [Molekulargenetik 29 - Adrenogenitales Syndrom, 21-Hydroxylase-Mangel (CYP21A2 Gen) (773)] Molecular Genetics 29 – Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency (CYP21A2 Gene) (773) [Molekulargenetik 29 - Adrenogenitales Syndrom, 21-Hydroxylase-Mangel (CYP21A2 Gen) (773)] 2023-10-23
PT provider ID (119881)

159161 Germany INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories INSTAND e.V., Society for Promoting Quality Assurance in Medical Laboratories Molecular Genetics 28 – CFTR Common Mutations (778) [Molekulargenetik 28 - CFTR Common Mutations (778)] Molecular Genetics 28 – CFTR Common Mutations (778) [Molekulargenetik 28 - CFTR Common Mutations (778)] 2023-10-23
PT provider ID (119881)

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