Bitgenia

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Acercamos la genómica a las personas Facilitamos el conocimiento de nuestro ADN para mejorar la calidad de vida. Revolucionamos la genómica y la bioinformática creando soluciones confiables, seguras y comprensibles para potenciar el nuevo paradigma de bienestar. Integramos con nuestras plataformas a los diferentes actores: hospitales, laboratorios, médicos, industria farmacéutica y personas. Procesando datos y brindando información de valor a medida. Somos un equipo multidisciplinario conformado por profesionales informáticos, médicos, biólogos, biotécnologos, genetistas e investigadores del CONICET. Somos líderes en el desarrollo de la medicina de precisión en Latinoamérica. Our goal is to improve people’s lifestyle by providing easy access to their DNA information. We revolutionise genomics and bioinformatics by creating reliable, safe and understandable solutions to enhance the wellness paradigm. With our in-house platform we integrate different stakeholders: hospitals, laboratories, doctors, pharmaceutical industry and consumers. We process data and provide customised and valuable information for your institution or company. We are a multidisciplinary team made up of IT professionals, doctors, biologists, biotechnologists, geneticists and researchers from CONICET. We are leaders in the development of precision medicine in Latin America.

Company Details

Employees
13
Founded
-
Address
Av. Alicia Moreau De Justo 1750, 3º H,argentina
Industry
Biotechnology Research
NAICS
Research and Development in Biotechnology (except Nanobiotechnology)
HQ
CABA, Buenos Aires
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Delayed Puberty Due to a WDR11 Truncation at Its N-Terminal Domain Leading to a Mild Form of Ciliopathy Presenting With Dissociated Central Hypogonadism: Case Report - Frontiers

Delayed Puberty Due to a WDR11 Truncation at Its N-Terminal Domain Leading to a Mild Form of Ciliopathy Presenting With Dissociated Central Hypogonadism: Case Report Frontiers

Inflammatory cutaneous lesions and pulmonary manifestations in a new patient with autosomal recessive ISG15 deficiency case report - Allergy, Asthma & Clinical Immunology

Inflammatory cutaneous lesions and pulmonary manifestations in a new patient with autosomal recessive ISG15 deficiency case report Allergy, Asthma & Clinical Immunology

Case report: Novel SIN3A loss-of-function variant as causative for hypogonadotropic hypogonadism in Witteveen–Kolk syndrome - Frontiers

Case report: Novel SIN3A loss-of-function variant as causative for hypogonadotropic hypogonadism in Witteveen–Kolk syndrome Frontiers

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