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Will Most Healthcare Apps Escape FDA Scrutiny?

PROTECT Act of 2014 proposes that Food and Drug Administration doesn't need to oversee "low risk" health IT products such as electronic health records and fitness apps.

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Two US senators want to give health IT software developers an easier path to consumers by turning the Food and Drug Administration's guidelines into a statute and moving oversight of these apps over to the National Institute of Standards and Technology (NIST).

The move would protect jobs, cut regulatory burdens, and allow the FDA to focus its limited resources on technologies and devices that need the department's scrutiny, the lawmakers say.

Under the Preventing Regulatory Overreach To Enhance Care Technology (PROTECT) Act of 2014, the FDA would no longer oversee "low risk health-IT" solutions such as electronic health records, scheduling software, and fitness apps, according to sponsors Sen. Angus King (I-Maine) and Sen. Deb Fischer (R-Neb.). The act also would eliminate a 2.3% medical device tax from EHRs, scheduling software, and wellness apps. The healthcare app market will reach $26 billion by 2017 and the mobile app market accounts for almost 500,000 jobs, the senators said.

[Is ObamaCare good for IT? Read 3 Ways Affordable Care Act Can Empower Health IT. ] 

"Not only is Health IT one of the most innovative and rapidly growing fields of technology in the country, but it's also fundamentally transforming the way we think about health care," said King in a statement. "As these technologies develop, it's critical to implement a clear, risk-based framework that would protect patient health and ensure that FDA rules are appropriately targeted to support and not stifle innovation. The PROTECT Act would provide important regulatory clarity that will safeguard patient safety, make the health care sector more efficient, and allow businesses across Maine and the nation to continue developing groundbreaking ideas."

The FDA regulates vaccines, drugs, and medical devices. In this age of mobile apps, 3D printing, and Internet of Things (IoT), the term "medical devices" has undergone a transformation and that goes to the heart of the PROTECT Act of 2014 -- and its October 2013 predecessor in the House of Representatives, the SOFTWARE Act.

Is it too difficult for healthcare app developers to get FDA approval today?
  Yes, there is too much regulation.
  Yes, another agency should oversee healthcare apps.
  No, the FDA's doing a good job.
  I don't know.
  Other. Please respond in comments.

In its final guidance on these apps, the FDA decided it would focus only on two types of apps. One is apps that "are intended to be used as an accessory to a regulated medical device," such as an app that lets a medical professional make a diagnosis by reviewing a medical image on a smartphone or tablet. The other is apps that "transform a mobile device into a regulated medical device," such as an app that turns a smartphone into an electrocardiography (ECG) machine. Each review takes about 60 days, wrote Christy Foreman, director, Office of Device Evaluation at the FDA's Center for Devices and Radiological Health, in a blog. Over the past decade, the center has reviewed about 100 health IT apps, she said.

That number will climb, argue PROTECT Act sponsors and supporters. Decreasing regulation -- and turning over what's left to a government organization well versed in working with software developers -- will streamline the process, allowing more ISVs and vendors to participate, hire more employees, pay more taxes, and extend the capabilities of this market, advocates say.

"Federal overregulation is one of the key challenges holding back entrepreneurs and job creators in Nebraska and across the country," said Fischer. "While economic growth remains sluggish, it's critical we prevent these costly and time-consuming bureaucratic hurdles from hurting one of the fastest growing sectors of our economy -- technology. The PROTECT Act increases regulatory efficiency over health IT to promote innovation, expand consumer access to information, and improve patient safety."

To date, IBM, AthenaHealth, the Software & Information Industry Association, the Newborn Coalition, and McKesson have voiced approval for the act.

"The current regulatory framework was largely developed before the rise of today's sophisticated information technologies, and it focuses on traditional discrete devices manufactured at a single site and physically shipped to distributors and users," said SIIA President Ken Wasch, in a blog. "With the rise of networked ecosystems and sophisticated software, this paradigm does not encourage today's innovations, let alone tomorrow's. Further, clarity is needed to encourage innovation and enables life-saving technologies to be brought to market in a timely manner."

He continued, "Fortunately, patient safety and product innovation are not mutually exclusive. SIIA supports the PROTECT Act because it takes necessary steps to establish a regulatory framework that provides for innovation without compromising safety. If enacted, the PROTECT Act will enable IT products and services to revolutionize health outcomes and lower costs for patients and providers."

Sen. Marco Rubio (R-Fla.) is an original co-sponsor of the act.

Biosense Technologies' uChek was one of the earliest health IT apps to fall under the FDA's scrutiny -- and fail. The Indian developer created a urinalysis app and "portable lab" that analyzes a user's urine for health problems such as diabetes. Biosense launched an Indiegogo campaign to raise funds and recruit users who will share their health data to meet the FDA's requirements.

Medical data breaches seem to show up on the 6 o'clock news almost every week. If you think it wouldn't happen to you -- or the financial impact will be minor -- think again. Download the Healthcare Data Breaches Cost More Than You Think report today. (Free registration required.)

Alison Diana has written about technology and business for more than 20 years. She was editor, contributors, at Internet Evolution; editor-in-chief of 21st Century IT; and managing editor, sections, at CRN. She has also written for eWeek, Baseline Magazine, Redmond Channel ... View Full Bio

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User Rank: Apprentice
2/14/2014 | 2:15:49 PM
Impact on stage 3 MU and PGHD
It'd be interesting to know what FDA's stand will be on part of regulations around stage 3 MU and Patient Generated Health Data(PGHD).
User Rank: Apprentice
2/13/2014 | 11:31:58 PM
Re: Modernizing Regs

Apps help us to monitor and track our behaviors, motivating us and providing real-time feedback to help us stay on a healthy track. They also allow you to have unprecedented access to your health record and to share information that's important to your health directly with your doctor. Why does the FDA need to get involved?

Than Nguyen


User Rank: Ninja
2/13/2014 | 4:53:48 PM
Surprised at the Numbers
I was surprised at the relatively small number of apps that have been scrutinized by the FDA to date. That said, surely the number will explode, if not this year in 2015, as more developers look to get into this market. Sixty days doesn't sound like much -- unless you're competing with a company that filed 59 days before you. 
User Rank: Author
2/13/2014 | 1:13:34 PM
Re: Modernizing Regs
Do more with less. We've all lived it for the past decade. The FDA can live it too. Figure out how to get it done with existing resources/money.
Lorna Garey
Lorna Garey,
User Rank: Author
2/13/2014 | 1:08:28 PM
Re: Modernizing Regs
On the face of it this seems to make sense. However, won't NIST need more manpower and a new set of expertise to evaluate HC-related apps? I don't see anything about beefing up that agency to handle these new duties.
User Rank: Author
2/13/2014 | 11:45:40 AM
Modernizing Regs
If it doesn't make sense to kill a regulation or regulatory body -- and food and drug approvals fall into that category -- it's reassuring to see the process being updated.
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