According to GlobalData’s medical device pipeline database, 136 Antepartum Monitors devices are in various stages of development globally. GlobalData’s report Antepartum Monitors 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, 39 are in active development, while the remaining 99 are in an inactive stage of development. There are 16 products in the early stages of development, and the remaining 23 are in the late stages of development.
Antepartum monitors refers to devices monitoring both maternal and fetal vital signs such as fetal/maternal heart rates, fetal ECG, maternal ECG, pulse oximetry, maternal BP, and uterine activity, during and before delivery. This is used on a routine basis throughout pregnancy. One unit refers to one antepartum monitor.
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 Antepartum Monitors 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 Antepartum Monitors devices. Overall, most of these Antepartum Monitors pipeline devices are being developed by private entities.
Key players involved in the active development of Antepartum Monitors include Adaltis, Roche Diagnostics International, Johns Hopkins University, Genome Diagnostics, Microbiologics, Qiagen, T2 Biosystems, SerImmune, University of Georgia and Washington University in St Louis.
For a complete picture of the developmental pipeline for Antepartum Monitors 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.
