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disrupts the health informatics industry by forever changing the way Pharma and medical device companies, physicians, payers and patients derive usable evidence from published clinical trials research. disrupts the health informatics industry by forever changing the way physicians, researchers, payers and consumers derive usable, accurate evidence from published clinical trials research. The resul
MedAware Systems announced today a major expansion of Neuromodulation device data in its SOHInfo (www.sohinfo.com) customer portal. The portal is populated with reported data from registries, published literature, and social media for all registered devices for Spinal Cord Stimulation, Peripheral Nerve Stimulation, Ganglia Dorsal Root Stimulation, RF Ablation, Parkinson - Deep Brain Stimulation, Sacral Stimulation – Incontinence, and others. Global regulatory reported data is provided on all manufacturers’ products for each product class. Learn more at:https://medawaresystems.com/wp-content/uploads/2021/12/MedAware-Systems-Expands-Post-Market-Surveillance-for-Neuromodulation-Devices.pdf
MedAware Systems Launches Automated Post Market Surveillance for Closure Devices
We've added another product group to our AI-powered SOHInfo Post Market Surveillance service. We are completing the service to cover all Class III and Class IIA devices. Learn more at :https://medawaresystems.com/wp-content/uploads/2021/07/MedAware-Systems-Launches-Automated-Post-Market-Surveillance-for-Closure-Devices.pdf
04/07/2021
From the article: "The MDR puts a higher emphasis on clinical data for medical devices and calls for increased scrutiny on the duty of manufacturers to continuously collect clinical data in the postmarket setting. Manufacturers are required to proactively collect and evaluate clinical data on the use of their devices."
Instantly and continuously delivering clinical data and postmarket data (including from social media) is the core of our Complete Product Monitoring System. See more at www.sohinfo.com
https://lnkd.in/eJKEqGg
How To Navigate Clinical Data Per EU MDR The EU MDR puts a higher emphasis on clinical data for medical devices and calls for increased scrutiny on the duty of manufacturers to continuously collect clinical data in the postmarket setting. Matthias Fink, MD, of TÜV SÜD America explains the MDR requirements surrounding clinical....
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