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DTSTAMP:20260524T113423Z
SUMMARY:FDA's Problem with Software Monsters
DESCRIPTION:Overview\n\nSoftware's level of complexity and use keeps e
 xpanding at exponential levels. Likewise, the potential risks to healt
 h and loss of privacy follow suit. Ransomeware attacks hold software p
 rograms hostage until you pay the culprit thousands of dollars.\nLife 
 supporting and life sustaining health software grinds to a halt. Extra
 cting personal healthcare information is another plague that has a hug
 e financial incentive for hackers. Your software is running on thin ic
 e. FDA looks at software based on the risk to health associated with t
 he software's use.\nCybersecurity problems for software for life susta
 in devices, wireless networks for patient manage and home use devices 
 open the gate for cyber intrusion, functional malware and total denial
  of access denial to an entire network of software, such as that used 
 in hospitals and clinics. Who will help you? This becomes a self-help 
 scenario; FDA and the FBI cannot protect you from the \"bad guy.\" An 
 equally disastrous problem involves interoperability failures.\nIf you
 r software does not cross the bridge of software communication, that s
 oftware becomes worthless. Wireless technology, mobile apps and home u
 se of software-based devices raise endless vulnerabilities. How you pr
 otect yourself and your customers in this swamp of disasters is critic
 al.\n\nWhy should you Attend\n\n\nFDA's regulatory controls\nCybersecu
 rity management\nRansomware attacks and recovery\nUse voluntary standa
 rds and NIST\nMobile apps\nWireless/home use software systems\n\n\nAre
 as Covered in the Session\n\n\nUnderstand FDA's risk-based regulatory 
 strategy\nLearn where FDA and you can find current technical help\nHig
 hlight the problems of interoperability and what you can do about it\n
 Familiarize yourself with the National Institute of Standards and Tech
 nology's (NIST) role in cybersecurity prevention and interoperability 
 considerations\nLearn about the FDA's increased use of voluntary stand
 ards\nClarify FDA's ongoing revision of mobile app regulation\n\n\nWho
  Will Benefit\n\n\nBusiness Planning Executives\nRegulatory Directors\
 nSoftware Design and Specification Developers\nReal time Software Perf
 ormance Auditors\nRecall Managers\nIn-house Legal Counsel\nCustomer Su
 pport and Service Directors\nContract Specialists\nBusiness Acquisitio
 n Managers\nHospital Risk Managers\n\n\nFor more information visit htt
 ps://medtechiq.ning.com/events/fda-s-problem-with-software-monsters
DTSTART;TZID=America/New_York:20190205T100000
DTEND;TZID=America/New_York:20190205T110000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://www.traininng.com/webinar/fda's-problem-with-soft
 ware-monsters-200597live?medtechiq_seo
URL:https://www.traininng.com/webinar/fda's-problem-with-software
 -monsters-200597live?medtechiq_seo
CONTACT:(510) 962-8903
ORGANIZER:Traininng.com LLC
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/702463962?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Joseph W
 ilcox":https://medtechiq.ning.com/profile/JosephWilcox
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