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Legal and Regulatory Issues Facing Users and Developers of Mobile Health Technology


Level: Advanced
Runtime: 91 minutes
Recorded Date: December 13, 2017
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$115

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Agenda

1:00 pm - 2:30 pm
  • mHealth overview
  • FDA Regulation of mHealth
  • When is mHealth regulated as a device?
  • What are the requirements for mHealth devices?
  • Reimbursement for digital health
Runtime: 1 hour and 31 minutes
Recorded: December 13, 2017

Description

The webinar will cover regulatory issues that arise in the use and development of mobile health technology (mHealth), with a focus on FDA regulation of apps, reimbursement for services delivered through mobile devices and apps, and state licensing issues that arise for health care professionals using mobile devices and apps.

Panelists will provide updates about the relevant legal and regulatory principles and developments facing lawyers who represent health care providers, investors, and technology developers who work with/develop mobile health technology.

This program was recorded on December 13th, 2017.

Provided By

American Bar Association
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Panelists

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Christina Kuhn

Associate
Covington & Burling LLP

Christina Kuhn advises medical device and biotech companies on a broad range of FDA regulatory strategy and compliance matters. She has experience with cutting-edge and complex medical technologies, including software and digital health products, oncology products, next-generation sequencing, diagnostics, and combination products.

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Philip Peisch

Special Counsel
Covington & Burling LLP

Phil Peisch helps clients navigate complex issues and disputes arising out of government-sponsored health care programs. Mr. Peisch has particular expertise regarding Medicaid, the Children Health Insurance Program (CHIP), and the Affordable Care Act's regulation of private insurance. He also counsels clients with respect to Medicare reiumbursement; state regulation of private health insurance; and other state and federal rules and policies governing the health care industry.

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