Webinar On FDA Regulation of Mobile Apps - PowerPoint PPT Presentation

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Webinar On FDA Regulation of Mobile Apps

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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? – PowerPoint PPT presentation

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Title: Webinar On FDA Regulation of Mobile Apps


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Contact Us 416-915-4458
Webinar On Webinar On FDA Regulation of Mobile
Apps

Presented By
Casper E. Uldriks
  Scheduled on Thursday, April 16, 2015 at 1300
Hrs
Hosting By Compliance Trainings
Please visit us at https//compliancetrainings.co
m
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Contact Us 416-915-4458
We Empower, You Comply!
FDA Regulation of Mobile Apps
Product Id
FDB1551
Category
Food, Drugs Biologics
Scheduled On
Thursday, April 16, 2015 at 1300 Hrs
Duration
60 Minutes
Speaker
Casper E. Uldriks
Login at https//compliancetrainings.com/si
teengine/Login.aspx
Webinar Description
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 FTCs and FDAs 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
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Areas Covered in the Session
  • FDA Strategy and Policy
  • Medical App Definition
  • Institutional and Home Use Risks
  • Cyber Security
  • Labeling Claims
  • Enforcement

Who Will Benefit
Practice Managers MD's and other Medical
Professionals Billing Companies Transcription
Companies IT Companies Answering Services Home
Health Coders Attorneys Any business associates
who work with medical practices or hospitals
Price Tags
Live Single Live For One Participant
189 Corporate Live For Max. 10 Participants
899 Recording Single REC For One Participant -
Unlimited Access for 6 Months 299
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Speaker Profile
Casper (Cap) Uldriks brings over 32 years of
experience from the FDA. He specialized in the
FDA's medical device program as a field
investigator, served as a senior manager in the
Office of Compliance and as an Associate Center
Director for the Center for Devices and
Radiological Health. He developed enforcement
actions and participated in the implementation of
new statutory requirements. He is recognized as
an exceptional and energetic speaker. His
comments are candid, straightforward and of
practical value. He understands how FDA thinks,
operates and where it is headed. Cap is the
President of Encore Insight LLC, a consulting and
training service for FDA law and operations.
To Register This Webinar Please Visit
https//compliancetrainings.com/SiteEngine/Produc
tDetailView.aspx?idFDB1551
Contact Us For Immediate Assistance _at_
416-915-4458 or Mail Us At uttam_at_compliancetrain
ings.com support_at_compliancetrainings.com
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