2016 - Webinar on FDA Regulation of Mobile Apps

Description :
The use of mobile apps as a medical device continues to mushroom. Approximately 85% of adults use cell phones. They offer a fertile field for mobile apps used for medical purposes, some good, some not. How do you decide which healthcare app is safe? Can someone hack an app you rely on for life supporting / life sustaining medical care? Yes. Patients and caregivers receive and install “app updates” with no idea what just happened and place themselves and even others in jeopardy. FDA has started to implement a regulatory approach and is overwhelmed now with that task. How much can FDA do? How will you know about the risks faced by the healthcare sector and you as an individual?
FDA is not the only regulatory stakeholder. The FTC exercises overlapping regulation. Are the two agencies in-sync with each other? Each agency is concerned about false or misleading claims. Marketers of standalone medical app software may have no clue about the FTC’s and FDA’s regulatory purview and enforcement authority over how a mobile app is marketed. That knowledge gap can be brutal, expensive and bring your business to a standstill.
Areas Covered in the Session :
FDA Strategy and Policy
Medical App Definition
Institutional and Home Use Risks
Cybersecurity
Labeling Claims
Enforcement
Who Will Benefit:
Regulatory Affairs Manager
Quality Assurance Manager
Software Design Engineers
Manufacturing Manager
Complaint Dept.
Hospital Risk Department
Software program marketers
IT security managers
Marketing managers
Home Healthcare Services
Healthcare Information Protection
Capital Venture Firms
Medical Device Consultants