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.

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Clinical Chemistry


70th AACC Annual Scientific Meeting & Clinical Lab Expo

Come and visit us at HORIBA Medical booth #3205 during AACC 2018, we will be happy to wecome you!

July 31 - August 2, 2018
McCormick Place, Chicago, Illinois
Visit us at booth #3205




HORIBA Medical Yumizen G Series

HORIBA Medical Yumizen G Range - My Companions for Coagulation Diagnostics



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Scientific Articles

An evaluation of the Yumizen H500 FBC analyser for near-patient testing with oncology patients

Kinal Amin, Kirolos Gabiows – Spire Pathology Services, Borehamwood, UK


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Evaluation of the Yumizen H500 FBC analyser for point of care testing for paediatric oncology patients

Daniel Boyland & Lydia Ingram - Lydia Ingram (University Hospital of Wales, Cardiff), UK


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Browse Products

HELO Solution
MoreHELO Solution
An innovative design solution covering all needs of high throughput automated hematology platforms
Quality Assurance Program
MoreQuality Assurance Program
Unique service support for quality and assurance
Quality Slide Program
MoreQuality Slide Program
Qualification tool for cytology staff in accordance with standard NF EN ISO 15189
Quality Control Program
MoreQuality Control Program
Online Interlaboratory Comparison Program

HORIBA Medical Quality Policy and Certification

HORIBA Medical QHSE Policy


The ISO 9001-2008 (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 14001-2004(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.