Best of 2018 in MedTech
Here are the most read articles of the year.
Tag Archives: software
Amazon’s Software Service Mines Medical Records, Aims to Improve Treatment and Lower Costs
Amazon Comprehend Medical uses machine learning to pull important medical information from patient records.
Medtech Cybersecurity State Not All Doom and Gloom, But Long Way to Go
Many device manufacturers don’t have the resources to adequately handle security risks.
Medical Device Software & Products Liability: Interoperability (Part III)
How software is changing the legal landscape for medical device manufacturers.
Why the EU Considers Prescription Support Software a Medical Device
SNITEM & Philips France vs. Health Minister: the ECJ defines the conditions under which software for assistance to the medical prescription can be qualified medical device within the meaning of the Directive.
Medical Device Software & Products Liability: The Homefront (Part II)
This second article in the three-part series looks at the use of software in medical devices in non-clinical settings, particularly the home environment. It addresses software’s role in the home healthcare trend, explains the software-related risks that arise from home-use products, and discusses what manufacturers can do to make these products safer.
Medical Software Regulations in Asia 2017
As standalone software becomes increasingly sophisticated, a number of regulatory bodies have begun to draft separate guidelines to ensure quality control, expedite product approval, and improve patient access to new technologies.
As standalone software becomes increasingly sophisticated, a number of regulatory bodies have begun to draft separate guidelines to ensure quality control, expedite product approval, and improve patient access to new technologies.
Safeguarding Medical Devices Against Cyber-Attacks
By adhering to FDA recommendations and leveraging the expertise of proven cyber testing methods, manufacturers can tackle known cybersecurity issues today while also attempting to anticipate concerns that may lie ahead.
Medical Device Software & Products Liability: An Overview (Part I)
How software is changing the legal landscape for medical device manufacturers.
Cybersecurity: FDA Calls for Firmware Update on Abbott’s Pacemakers
The corrective action is intended to reduce the risk of patient harm as a result of cybersecurity vulnerabilities in the products.
