According to GlobalData’s medical device pipeline database, 43 Hepatitis C Point of care (POC) Tests devices are in various stages of development globally. GlobalData’s report provides an overview of the segment’s pipeline landscape and offers detailed analysis of its products. Buy the report here.

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Of these devices, 24 are in active development, while the remaining 19 are in an inactive stage of development. There are 18 products in the early stages of development, and the remaining six are in the late stages of development.

Hepatitis C Test Kits are used for the point-of-care detection of Hepatitis C virus (HCV), an RNA virus of the family Flaviviridae that leads to chronic hepatitis, resulting in cirrhosis, but carriers can be asymptomatic for decades.

Innovations in the medical devices sector are linked to the development of new approaches, processes, or technologies for treating, diagnosing, and managing disease in response to demand from healthcare for better patient outcomes and reduce healthcare costs.

Based on an analysis of GlobalData’s Medical Intelligence Center pipeline product database, these actively developed Hepatitis C Point of care (POC) Tests pipeline devices are all expected to be approved within the next ten years.

Currently, private organizations, public entities and institutions are working on the development of Hepatitis C Point of care (POC) Tests devices. Overall, most of these Hepatitis C Point of care (POC) Tests pipeline devices are being developed by private entities.

Key players involved in the active development of Hepatitis C Point of care (POC) Tests include Chembio Diagnostic Systems, Qoolabs, Quidel, Redbud Labs, SD Biosensor, Sensible Diagnostics, Senzo, SLS Cell Cure Technologies, Tango Biosciences and University of California Irvine.

For a complete picture of the developmental pipeline for Hepatitis C Point of care (POC) Tests devices, buy the report here.

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article. 

The medical devices pipeline data used in this article were obtained from the Medical Pipeline Products Database of GlobalData’s Medical Intelligence Center. The Pipeline Products database is a is a comprehensive source of information on medical devices, it covers 39K products which are in development stage and intended for diagnosis, treatment, and management of diseases/conditions/symptoms directly or indirectly. The pipeline products included in the database are sourced from reliable and authenticated sources, such as company websites, SEC filings, conference presentations, analyst presentations, news releases, clinical trial registries, and grants. The information is collected by following systematic research techniques and proprietary methodology.