Mobile Medical Applications: Trends and Regulations in US & Globally - Webinar By GlobalCompliancePanel by globalcompliancepane


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									GlobalCompliancePanel                                                 Your Gateway to Regulatory Compliance

Live Webinar on

Mobile Medical Applications: Trends and Regulations in US &

Date: Wednesday, March 27, 2013                                       Time: 10:00 AM PST | 01:00 PM EST

Duration: 90 Minutes             Location:   Online          Instructor: Kosta Makrodimitris

Course "Mobile Medical Applications: Trends and Regulations in
US & Globally" has been pre-approved by RAPS as eligible for up to
1.5 credits towards a participant's RAC recertification upon full
                                                                                     Register Now

m-Health is the field of using mobile devices to provide services and support for medicine,
healthcare and public health. It’s a fast growing field globally that targets doctors, patients,
consumers, managers and IT groups among others. The trends for this field are showing a lot of
investments and high revenues for the coming years.

Areas covered in the session:

    l   Overview of Health IT and mobile industry
    l   Basic of mobile applications for health
    l   Medical devices related to mobile health
    l   Draft guidances in mobile medical apps(FDA 2011-2012)
    l   FDA Safety & Innovation Act and m-Health
    l   Patient and Consumer health information and security
    l   Coming FDA final guidelines and DHHS actions
    l   Mobile health standards
    l   Mobile Health globally(WHO, EU)
    l   Future of m-Health industry and workforce

Who Will Benefit:                                         About Speaker

                                                          Kosta Makrodimitris
    l   Management
                                                          Health IMS Consultant, K
    l   Health IT Managers                                Makrodimitris
    l   Research and Development                          Kosta Makrodimitris is the principal
                                                          for K Makrodimitris that specializes in
    l   Regulatory Affairs
                                                          Health IT & BIO business
        Personnel                                         development, eHealth education,
    l   Quality assurance/quality                         Health Information policy.
        Control Personnel                                 He is certified on EHR/PHR, Clinical
                                                          Trials, Biotech/Drug Development,
    l   Auditors and Inspectors
                                                          and trained in US FDA/DHHS laws,
    l   Entrepreneurs                                     regulations (devices, foods, drugs,
    l   Investors                                         personalized health).   ...more

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