Health IT Product News Report
Allied Market Reseach reports that the US Health Care Information Technology market was evaluated at $61,018 million in 2017, and is estimated to reach $149,178 million by 2025, at a CAGR of 11.7% during the forecast period. The industry is driven by growing demand for improved patient safety and patient care as well as increase in government initiatives to promote and adopt health IT.
Data Bridge Market Research reports the market drivers and growth can be attriuted to the increase in technological know-how, growing volume of patient data, and demand for quick and efficient healthcare processes and systems will help in driving the growth of the healthcare IT market. Increasing digitization in the healthcare industry and demand for value based care and rising cost of provision of healthcare services coupled with the increasing number of healthcare facilities will likely accelerate the growth of the healthcare IT market in the forecast period of 2020-2027.
And finally over 120 companies are found on the newest Inc. 5000 2020 list of fastest growing private companies. Several of those in the top 200. The list is ranked according to percentage revenue growth when comparing 2016 and 2019.
Read all our product news reports. Here is a snapshot of health IT product news being announced.
https://www.healthcarenowradio.com/tag/product-news/
Health IT Product News:
DrFirst’s Medication Management Suite and Backline Care Collaboration Platform Earn High Marks from Customers in KLAS First Look Report
Healthcare pioneer DrFirst (@DrFirst) announced how customers rate its Medication Management Suite (MMS) and Backline care collaboration platform, as reported in KLAS Research’s First Look report.
Experity Unveils New Urgent Care EMR/PM Designed to Power the Future of On-Demand Care
Experity (@experityhealth), the national provider of on-demand care solutions, announced its newest electronic medical record and practice management solutions (EMR/PM). Experity EMR/PM was developed with leading urgent care organizations across the U.S. to support urgent care-specific needs as they evolve to meet growing patient and provider expectations while delivering quality, high-velocity on-demand care.
Jump Technologies introduces Case Companion to help hospitals optimize clinical workflows and control costs in the OR
Jump Technologies (@JumpTechNews), a hospital supply chain solutions provider, announced the launch of Case Companion, a clinical solution designed to help hospital staff reduce duplicate documentation, improve real-time charge capture in the OR, control surgical material costs, and avoid costly stockouts.
Belong.Life Launches i-Belong High-Engagement Platform, Allowing Providers, Health Plans, Advocacy Groups and Other Health Ecosystem Players to Easily Build Self-Managed Online Patient Communities
Belong.Life (@Belong_Life), a developer of global patient engagement and research platforms, and the largest health networks for cancer, multiple sclerosis and other diseases, announced the launch of i-Belong – Connecting Communities. i-Belong is a self-managed platform for health ecosystem players to build customizable communities and social networks. i-Belong will offer payers, providers, pharmaceuticals and patient advocacy groups personalized and configurable engagement tools to enable organizations to serve more patients effectively and efficiently.
Greenway Health transforming EHR platforms, Intergy and Prime Suite, to meet evolving ambulatory care practice needs
Greenway Health (@greenway), a health information technology services provider, announced the company will double its investment in its two core electronic health record (EHR) platforms, Intergy and Prime Suite, to better meet the evolving needs of clients and the industry. The company’s client-centric product development approach will include a number of client requested enhancements to further improve clinical workflows, reduce cognitive load, and improve patient care and outcomes. Greenway believes healthcare organizations deserve more than off-the-shelf technology services and solutions – particularly as the landscape of the industry evolves.
FDS Amplicare Announces New Vaccine Registry Reporting & Querying Capabilities
FDS Amplicare (@FDSRx) announced new vaccine registry reporting and querying capabilities, enabling users to more easily submit patient vaccination information to required state registries. The new software add-on streamlines the overall vaccination process and moves important patient information into the hands of vaccine administrators more quickly and efficiently and better enabling community pharmacists — especially in rural and underserved areas — to deliver life-saving vaccines.
Telemedicine Product News:
19Labs adds GALE | VisualVitals: Deviceless Vital Sign Measurement to GALE Point-Of-Care eClinics
19Labs (@19_labs), the creator of the GALE remote point-of-care open platform, announced the launch of GALE | VisualVitals which measures a patient’s vital signs using only a tablet’s built-in camera. The technology makes GALE the world’s first platform that integrates FDA-approved devices (e.g. blood pressure, pulse oximeter, etc.) together with the latest machine learning visual technologies to assess patient health and wellness. Clinicians can leverage both FDA-approved devices and GALE | VisualVitals to diagnose patients during telehealth calls. Patients can use GALE | VisualVitals on their own as well, to monitor well-being at their convenience.
FDA Medical Devices approved in August 2021
The FDA regulates medical devices sold in the United States to assure their safety and effectiveness. Medical devices range from simple tongue depressors and hospital gowns to complex programmable pacemakers and robotic surgical systems. Their Medical Device Product Classification database lists over 6,000 types of medical devices regulated by FDA’s Center for Medical Devices and Radiological Health (CDRH) and the classification assigned to each type. Depending on the device classification, along with other factors, federal regulations (such as the Code of Federal Regulations, Title 21) define requirements that must be fulfilled for CDRH to approve or clear devices sold in the United States.
Here are the recently approved devices for August.
