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Spiritus Partners post-market surveillance and adverse event analytics, compliance reporting and consulting for medical device manufacturers and healthcare providers

Hospitals, healthcare systems, and medical device manufacturers post-market surveillance, adverse event analytics, compliance reporting and consulting to improve patient safety and reduce risks and costs of quality events across the supply chain. Addresses FDA, CDRH and EU MDR regulatory requirements for quality management systems and recalls

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Spiritus Partners post-market surveillance and adverse event analytics, compliance reporting and consulting for medical device manufacturers and healthcare providers | spirituspartners.com Reviews
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Hospitals, healthcare systems, and medical device manufacturers post-market surveillance, adverse event analytics, compliance reporting and consulting to improve patient safety and reduce risks and costs of quality events across the supply chain. Addresses FDA, CDRH and EU MDR regulatory requirements for quality management systems and recalls
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Spiritus Partners post-market surveillance and adverse event analytics, compliance reporting and consulting for medical device manufacturers and healthcare providers | spirituspartners.com Reviews

https://spirituspartners.com

Hospitals, healthcare systems, and medical device manufacturers post-market surveillance, adverse event analytics, compliance reporting and consulting to improve patient safety and reduce risks and costs of quality events across the supply chain. Addresses FDA, CDRH and EU MDR regulatory requirements for quality management systems and recalls

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Adverse Event Analytics and Reporting for Medical Devices

http://www.spirituspartners.com/new-page

Over the Horizon Leadership. Known for blending foresight with pragmatism, Susan's career on Wall Street and in banking has spanned sales, product development, strategic sourcing, and corporate development. Most recently, she's served as Head of Risk for a leading provider of enterprise software and services for global banks and money managers. Susan is a graduate of Princeton University. Gail baura, PhD. Director of Engineering Science - Loyola University Chicago. Andrea belz, Phd. MICHAEL CHELLSON, RAC.

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Adverse Event Analytics and Reporting for Medical Devices

http://www.spirituspartners.com/news

Healthcare Blockchain Summit (Washington, DC March 20-21, 2017). 3rd Annual Global Postmarket Surveillance of Medical Devices (Alexandria, VA Feb. 23-24, 2017). ScotChain16 (Edinburgh, Scotland Nov. 11, 2016). Distributed: Health (Nashville, TN Oct. 2, 2016) - "Blockchain in Business". Internet2 CINC Up (Webinar Dec. 6, 2016) - "Blockchain in Education and Research".

3

Adverse Event Analytics and Reporting for Medical Devices

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What Can Consumer Wearable Do? The rise of consumer health wearables: promises and barriers," PLOS medicine. February 2, 2016 By Lukasz Piwek, David A. Ellis, Sally Andrews, Adam Johnson. Alaris SYRInge Pump module (Model 8100 and ail sensor kits by carefusion: class 1 recall - alarm error). Audience: Risk Manager, Nursing. Recent News and Notices. Medtronic recalls synchromed ii and synchromed el implantable drug infusion pumps due to failure of priming bolus - update related to may 2013 recall. Https:/...

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Adverse Event Analytics and Reporting for Medical Devices

http://www.spirituspartners.com/how-we-help

Device Registry and Chain of Custody. Track and Trace" Chain of Custody for a Medical Device Across Its Lifecycle and the Ecosystem. Has combined proven enterprise-class software and promising emerging technologies to create a permissioned platform as a lightweight overlay of existing device registries and reporting databases. A cloud-based SaaS offering,. Data Visualizations, Drill Downs and Tailored Reporting. Patient safety is central to everything we do.

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Adverse Event Analytics and Reporting for Medical Devices

http://www.spirituspartners.com/projects

You're caught in a tough place. As a clinical governance, quality management, or risk management professional, you're responsible for patient safety at a time when demands for greater efficiency and even cost reductions are growing. To make things worse. Innovation is a two-edged sword. Medical devices designed to manage chronic, non-communicable diseases are increasingly. Instrumented, interoperable, connected and intelligent. When something bad happens,.

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Spiritus Partners post-market surveillance and adverse event analytics, compliance reporting and consulting for medical device manufacturers and healthcare providers

Wired for Patient Safety. Medical devices are increasingly. Instrumented, interoperable, connected and intelligent. With such advances, though, come an increased probability of adverse events - injuries, complications, disabilities and deaths. In a value-based setting, health systems and healthcare providers are bearing more of the costs and risks of these incidents - financial, legal, regulatory and reputational. Improve Post-market Surveillance and Adverse Event Management. Our cloud-based software and...

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