The use of mobile apps as a medical device continues to mushroom.  Approximately 85% of adults use cellphones. 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 PolicyMedical App DefinitionInstitutional and Home Use RisksCybersecurityLabeling ClaimsEnforcementWho Will Benefit:Regulatory Affairs ManagerQuality Assurance ManagerSoftware Design EngineersManufacturing ManagerComplaint Dept.Hospital Risk DepartmentSoftware program marketersIT security managersMarketing managersHome Healthcare ServicesHealthcare Information ProtectionCapital Venture FirmsMedical Device ConsultantsPrice Tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct,  Mississauga, ON L5V 2V5,  Canada  Customer Support : #416-915-4458