Medical

Medical

The HORIBA Medical Segment designs, develops and distributes worldwide, in vitro diagnostic systems mainly destined for biological analysis in medical laboratories. These automated analyzers meet the needs of various users including patients, doctors, private laboratories, clinics and university hospitals. HORIBA expertise in in vitro diagnostics is one of the most respected in hematology worldwide and contribute today to the health of tomorrow.

Hematology

Coagulation

Clinical Chemistry

Automation

Division_-_Automation

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HORIBA Medical Brings Malaria Screening in Routine Hematology

Based on innovative ‘data mining’ techniques and combined with Full Blood Count, the Malaria suspicion flag is optionally available on both the ABX Pentra XL 80 and Pentra XLR.

 

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HORIBA Medical launches their new parameter, Yumizen D-Dimer, for deep vein thrombosis and pulmonary embolism diagnosis on the Yumizen G Hemostasis range

HORIBA Medical announces the availability of a D-Dimer reagent for their semi-automated Hemostasis instruments.

 

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EuroMedLab 2019

23rd IFCC-EFLM European Congress of Clinical Chemistry and Laboratory Medicine

 

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HORIBA Medical Corporate Clip 2019

 

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Yumizen

HORIBA Medical presents “Yumizen”, the new brand for all future analyzers and solutions including Hematology, Clinical Chemistry and Care Products.

Choose Yumizen, you will stay zen.

 

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Point of Care Testing

World exclusive CRP hematology combined solutions at the point of care.

 

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Scientific Articles

Evaluations and testimonials on Yumizen analyzers 

 

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HORIBA Medical Quality Policy and Certification

HORIBA Medical QHSE Policy

 

The ISO 9001-2015 (Quality Management Standard) is the internationally recognised standard for the quality management of businesses. It applies to the processes that create and control the products and services an organisation supplies. It prescribes systematic control of activities to ensure that the needs and expectations of customers are met.

 

The ISO 14001-2015 (Environmental Management Standard)
is the internationally recognised standard for the environmental management of businesses. It prescribes controls for those activities that have an effect on the environment. These include the use of natural resources, handling and treatment of waste and energy consumption.

 

The ISO 13485-2012 is a quality system standard designed specifically for medical device companies. It supplements ISO 9001 and has many of the same requirements. However, there are additional requirements for process control, design control, retention of records, accountability, traceability and more.

 

The OHSAS 18001-2007 (Occupational Health and Safety Assessment Series) certification is designed to help organisations formulate occupational health and safety policies and objectives.