6-Hour Virtual Seminar on FDA's Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use
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Website https://www.globalcompliancepanel.com/virtual-seminar/-10390LIVE?channel=ourglocal-march_2020_SEO |
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Deadline: March 16, 2020 | Date: March 16, 2020
Venue/Country: Online Event, U.S.A
Updated: 2020-01-17 21:18:54 (GMT+9)
Call For Papers - CFP
The complexity and vulnerability of software is expanding exponentially, so fast that Congress removed some device software from FDA’s jurisdiction. The remaining software regulated by FDA presents a degree of a risk to health that creates a public health concern. Part of that risk involves the intentional activity that can conflict, intrude or destroy software. The problems are taking center stage in the "healthcare software" dialogue.What issues can compromise or defeat the functional use of your software? Poor cybersecurity programs, lack of interoperability with third-party software, the wave of unmanageable apps and wireless home use technology. Original software design for an intended use is only the first step, the next design step is thinking about how someone can make your software worthless.Why you should attendFDA's changing regulatory controlsCybersecurity management by design, oversight and preventive actionRansomware attacks and recoveryUse voluntary standards and NISTMobile apps regulated and those not regulatedWireless/home use software systems and human factorsWho Will BenefitBusiness Planning ExecutivesRegulatory DirectorsSoftware design and specification developersReal time software performance auditorsRecall managersIn-house Legal CounselCustomer support and service directorsContract SpecialistsBusiness acquisition ManagersHospital Risk Managers
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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