FDA and cloud-based medical device

Digital Health Criteria – FDA

https://www.fda.gov/MedicalDevices/DigitalHealth/ucm575766.htm

Sep 22, 2017 – Software run on a hardware medical device is a SaMD when not part of the intended use of the hardware medical device. … A picture archiving and communications system consists of cloudbased, web-accessible software that analyzes cardiovascular images acquired from magnetic resonance (MR) …

Medical Device Data Systems – FDA

https://www.fda.gov/MedicalDevices/ProductsandMedicalProcedures/GeneralHospital…

Jun 9, 2017 – The 21st Century Cures Act (12/13/2016) clarified FDA’s regulation of medical software. The new law amended the definition of “device” in the Food, Drug and Cosmetic Act to exclude certain software functions. The FDA is currently developing draft guidance for public comment to help industry and FDA …

Medical Devices / Radiation-Emitting Products | FDA Voice

https://blogs.fda.gov/fdavoice/index.php/…/medical-devices-radiation-emitting-produ…

Our science-based and patient-centered regulatory approach also extends to medical devices, where we’ve focused on a life-cycle approach to product development. This has allowed us to streamline clinical development protocols without compromising on our commitment to rely on rigorous evidence. By carefully …

Medical Devices > General Principles of Software Validation … – FDA

https://www.fda.gov/MedicalDevices/ucm085281.htm

Jun 14, 2017 – This document is based on generally recognized software validation principles and, therefore, can be applied to any software. For FDA purposes, this guidance applies to any software related to a regulated medical device, as defined by Section 201(h) of the Federal Food, Drug, and Cosmetic Act (the Act) …

[PDF]Final Guidance on Medical Device Accessories: Describing … – FDA

https://www.fda.gov/downloads/Training/CDRHLearn/UCM540929.pdf

Feb 2, 2017 – Final Guidance on Medical Device Accessories: Describing Accessories and Classification. Pathway for New Accessory … therefore also for software as a medical device or SaMD, this guidance is applicable to the …… based or cloudbased software uses support a service activity or a workflow, to support a …

Precision Medicine – FDA

https://www.fda.gov/ScienceResearch/SpecialTopics/PrecisionMedicine/default.htm

Dec 21, 2017 – The Precision Medicine Initiative seeks to identify genetically-based drivers of disease in order to develop new, more effective treatments. … The FDA created precisionFDA, a cloudbasedcommunity research and development portal that engages users across the world to share data and tools to test, pilot, …

First FDA Approval For Clinical Cloud-Based Deep Learning In …

https://www.forbes.com/…/first-fda-approval-for-clinical-cloud-based-deep-learning-i…

Jan 20, 2017 – The FDA approval of a cloud based machine learning application to be used in a clinical setting to help physicians understand how a heart is functioning signals a major breakthrough. Cutting examination time from up to an hour to just 15 seconds paves the way for more AI algorithms inhealthcare.

Arterys Receives FDA Clearance For The First Zero-Footprint Medical …

https://www.prnewswire.com/…/arterys-receives-fda-clearance-for-the-first-zero-footp…

Jan 9, 2017 – SAN FRANCISCO, Jan. 9, 2017 /PRNewswire/ — Arterys, a pioneer in cloudbased medicalimaging software, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its Arterys Cardio DLTM application. Arterys Cardio DLTM is the first technology to be cleared by the FDA …

The Impact of Cloud Computing on FDA’s Regulation of Medical …

https://www.fdalawblog.com › Legislation

Feb 14, 2013 – Given the complexity with using cloud computing services in FDA regulated medical products, it is critical to carefully consider the regulatory impact of incorporating such services. Sheppard Mullin has expertise in the legal and regulatory issues surrounding cloud based services, including when using …

Leveraging Cloud-based VDI for Medical Devices – ClearDATA

https://www.cleardata.com › knowledge hub › Blog

Medical devices improve and save lives, but security risks around them are increasing, putting patients and providers at risk. Medical devices help improve patient outcomes and can save lives, and dozens of new technologies are approved by the U.S. Food and Drug Administration (FDA) each year. However, the …

Leave a Reply