Wednesday, March 27 2013 at 10:00 AM (Get Tickets)
Location:
Online Training
Livermore Common
Fremont,CA, CA 94539
United States
Event Description:
Overview: 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.
Several government agencies in US (FDA, FTC, FCC, ONC) and worldwide are preparing guidances and regulations to protect patient safety and privacy of health information. In addition there are other standards development organizations who try to harmonize efforts globally to propose mHealth standards for new mobile health systems. The topic and the field of m-Health and mobile medical applications is multidisciplinary since multiple stakeholders are involved and have a lot of interests.
Why Should You Attend: This webinar will provide the new and expected regulations and discuss their effects on the use of mobile medical application for devices. We will explain the policies, predict coming regulations and discuss how mobile Health (m-Health) industry will be affected. We will explore the current emerging m-Health landscape in US and globally.
All functional groups who have responsibility or need to understand the new technologies and regulations of mobile medical applications and biomedical software for medical devices and smartphones should attend.
Areas Covered in the Session:
Overview of Health IT and mobile industry
Basic of mobile applications for health
Medical devices related to mobile health
Draft guidances in mobile medical apps(FDA 2011-2012)
FDA Safety & Innovation Act and m-Health
Patient and Consumer health information and security
Coming FDA final guidelines and DHHS actions
Mobile health standards
Mobile Health globally(WHO, EU)
Future of m-Health industry and workforce
Who Will Benefit:
Management
Health IT Managers
Research and Development
Regulatory Affairs Personnel
Quality assurance/quality Control Personnel
Auditors and Inspectors
Entrepreneurs
Investors
Kosta Makrodimitris, PhD, CF-FDA, CP-EHR, is Biomedical/Health Informatics Advisor, Author & Strategist.
Dr. Makrodimitris is the principal for K Makrodimitris that specializes in Health IT & BIO business development, eHealth education, Health Information policy.
USA
GlobalCompliancePanel,
Livermore Common, Fremont, CA, 94539
USA Phone:800-447-9407
Fax: 302-288-6884
webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com