Genedrive advances after signing distribution deal with Sysmex Europe
genedrive and Sysmex Europe believe there is a major opportunity to support tackling the global burden of the hepatitis C disease
Company
LON:GDR
genedrive plc is a pharmacogenetic testing company developing and commercialising a low cost, rapid, versatile and simple to use point of need pharmacogenetic platform for the diagnosis of genetic variants. This helps clinicians to quickly access key genetic information that will aid them make the right choices over the right medicine or dosage to use for an effective treatment, particularly important in time-critical emergency care healthcare paradigms.
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genedrive and Sysmex Europe believe there is a major opportunity to support tackling the global burden of the hepatitis C disease
The UK blue chip index closed at 7,526, well below the session peak of 7,557.00 and close to the day’s low of 7,531.48
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The hepatitis C assay provides decentralised molecular testing to support the identification of patients who could benefit from direct acting antiviral therapy
The blue chip index closed out almost 36 points higher at 7,413
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Genedrive is further developing its handheld device to detect a broader range of biohazard targets
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Genedrive submitted its Genedrive HCV ID kit for CE IVD certification back in March and said today it expects to hear back in the “near future”
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Genedrive’s HCV assay provides on-the-spot results in just 90 minutes direct from a very small plasma sample.
Regulatory sign-off fires starting pistol on the commercial launch in Europe, Africa, EU Medical Devices Directive awarded CE IVD certification, molecular diagnostics, Europe, Africa, Sysmex
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The receipt of CE IVD certification under the EU Medical Devices Directive would green-light the commercialisation of the product in the European Union.
The studies were performed at Queen's Medical Centre and Institut Pasteur
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Chief executive David Budd said: "We are making good progress towards realising the proven potential of the Genedrive platform in a range of applications through our own programmes and partnerships.”
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Officials will assess the technology's potential to check for hazards such as biological warfare agents.
It has been awarded what’s called CE-IVD certification, that’s the official CE mark for an in-vitro diagnostic medical device.
The year has seen us take further significant strides towards realising the potential of the Genedrive platform to bring the strength of hospital-based, central laboratory diagnostics close to the point of need and near patient setting - ch
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