FDA`s Oversight of Mobile Medical Applications (`apps`) for Use on Smartphones and Similar Mobile Devices 2013
10 Sep 2013
Webinar
Description
Topics
The criteria for distinguishing between regulated and unregulated mobile medical apps
FDA’s regulation of mobile medical apps
The July 2011 Mobile Medical App Draft Guidance Document
Discussion of the responsibilities of a regulated entity
Identification of application FDA regulations, guidance documents and other relevant documents
What regulatory requirements must a manufacture comply with to market a regulated app
Who should Attend
Medical device and Biotech Companies, Start-ups, Foreign Device Manufacturers, Importers, Device Reprocessors; Mobile and Smartphone Companies; the Telecom Industry
Regulatory Affairs Professionals, Managers, Consultants, Scientists, Research Analysts, State Policy Officials, Insurers focusing on Representations & Warranties Insurance; Investment Analysts; Venture Capitalists
Financial analysts and investors watching the pharmaceutical, life sciences and biotech industries
Past Events
FDA`s Oversight of Mobile Medical Applications (`apps`) for Use on Smartphones and Similar Mobile Devices 2013 - 10 Sep 2013, Webinar (27322)
Important
Please, check "FDA`s Oversight of Mobile Medical Applications (`apps`) for Use on Smartphones and Similar Mobile Devices" official website for possible changes, before making any traveling arrangements
