Date: | January 18, 2018 - 9:00am - January 19, 2018 - 4:30pm |
Timezone: | (GMT-05:00) Eastern Time (US & Canada) |
Location: | CA, 92101, United States |
Website for Event: | http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901393SE... |
Topic: | Health Education |
Description: | Course "FDA's Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Software's level of complexity and use is expanding at exponential levels. Likewise, the potential risks to health follow suit. Ransomeware attacks hold your software hostage until you pay hundreds or thousands of dollars. Life supporting and life sustaining healthcare grinds to a halt. Extracting personal healthcare information is another plague that has a huge financial incentive for hackers. Your software is running on thin ice. Why you should attend: For decades, firms have experienced serious problems with software and have been at a loss to make a well-informed follow up. Software problems represent one of the most common root causes for recalls that are associated with deaths and serious injuries beyond what should be necessary to quantify. FDA sees firms revise software only to create more problems rather than solve them. The infusion pump industry is a classic example that drove FDA to implement a new rigorous paradigm for premarket review and performance criteria evaluation. Topics: Who Will Benefit: Agenda: Day 1 Schedule 9:00 am - 10:15 am Speaker Casper (Cap) Uldriks brings over 32 years of experience from the FDA. He specializes in the FDA's medical device program as a field investigator, served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements. He is recognized as an exceptional and energetic speaker. His comments are candid, straightforward and of practical value. He understands how FDA thinks, operates and where it is headed. Cap is the President of Encore Insight, LLC, a consulting service for FDA matters. Location: San Diego, CA Date: January 18th & 19th, 2018 and Time: 9:00 AM to 4:30 PM Price: Contact us today! NetZealous LLC DBA GlobalCompliancePanel Registration Link - http://www.globalcompliancepanel.com/control/globalseminars/~product_id=... Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/ |
Contact Name: | Event Manager |
Contact Email: | john.robinson@globalcompliancepanel.com |
Contact Phone: | 800-447-9407 |