Healthcare Training 2020 - 6-Hour Virtual Seminar on FDA's Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use

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 attend
FDA's changing regulatory controls
Cybersecurity management by design, oversight and preventive action
Ransomware attacks and recovery
Use voluntary standards and NIST
Mobile apps regulated and those not regulated
Wireless/home use software systems and human factors
Who Will Benefit
Business Planning Executives
Regulatory Directors
Software design and specification developers
Real time software performance auditors
Recall managers
In-house Legal Counsel
Customer support and service directors
Contract Specialists
Business acquisition Managers
Hospital Risk Managers