Date :
Place : United States, Boston, ma
Contact Person:Eevnt Manager
Description:
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. The FDA looks at software in one of three ways: Standalone, such as for a mobile app; device-based software used to control a device's performance, or simply electronic records. FDA's risk classification will gradually clarifyDeadline for abstracts/proposals : 4th December 2017
Organized By :NetZealous DBA as GlobalCompliancePanel
Keynote Speakers : Casper Uldriks ex-FDA Expert and former Associate Center Director of CDRH 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 excep
Conference Highlights :Regulatory Affairs Quality Assurance Software Design Engineers Manufacturing Complaint Dept. Hospital Risk Dept. Own label marketers
Venue :Boston, MA, United States
Check the event website for more details.