According to GlobalData’s medical device pipeline database, 61 Colorectal Cancer Screening Tests devices are in various stages of development globally. GlobalData’s report Colorectal Cancer Screening Tests 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, 50 are in active development, while the remaining 11 are in an inactive stage of development. There are 13 products in the early stages of development, and the remaining 37 are in the late stages of development.
This segment includes sub-segments Guaiac Fecal Occult Blood Test (gFOBT) Kits, Immunochemical Fecal Occult Blood Test (iFOBT or FIT) Kits, Fecal DNA Test Kits and Other Colorectal Cancer Screening Tests.
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 Colorectal Cancer Screening 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 Colorectal Cancer Screening Tests devices. Overall, most of these Colorectal Cancer Screening Tests pipeline devices are being developed by private entities.
Key players involved in the active development of Colorectal Cancer Screening Tests include Guardant Health, VolitionRX, Chinese University of Hong Kong, Chinese University of Hong Kong, Acuamark Diagnostics, Advanced Marker Discovery, Anixa Diagnostics, Arbele, Augusta University and Bar Harbor BioTechnology.
For a complete picture of the developmental pipeline for Colorectal Cancer Screening 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.
