In February, 2012, in a blog post provocatively titled “An App for That, But For How Much Longer?”, PhRMA’s Kate Connors agreed with a Washington Times op-ed piece that suggested the FDA will soon require apps such as medication prescription renewal reminders and blood glucose level tracking functions to be regulated as medical devices. In my own blog post, I cited this post as “FDA Mobile Regulatory Fear Mongering.” You can read my blog post (here) to see why or you can read “No, the FDA is not assaulting mobile technology, Washington Times editorial misguided” published by iMedicalApps.
More recently, I suggested that The Best Defense Against Zealous FDA Regulation is Self-Regulation (see “My POV Regarding Regulation of Pharma Mobile Medical Apps“).
I wonder how many people feel as I do. So, I posted the Regulation of Pharma Health Apps Survey to find out (see the survey embedded at the end of this post). This survey asks your opinion regarding several issues faced by pharma companies when developing mobile applications (apps) for physicians and consumers. Issues include impact of regulation by FDA, privacy, trust, accuracy, and 3rd-party certification as well as industry self-regulatory guidelines.
I recently interviewed Happtique CEO Ben Chodor who said “There are tens of thousands of medical, health and fitness apps on the market and their sheer number makes it difficult for health care professionals and consumers to locate apps that operate reliably, are based on valid information, and safeguard users’ information” (listen to the podcast: “Taming the ‘Wild West’ of Mobile Health“).
Sooner or later, IMHO, Congress is going to be investigating mobile health apps to see if further regulations — not just FDA regulations — are required. IMHO, the pharmaceutical industry (i.e., PhRMA) should differentiate itself from the “wild west” developers by being pro-active in issuing Guidelines for Mobile Health Apps Developed by the Pharmaceutical Industry in much the same manner as it developed other self-regulatory guidelines such as the DTC Guiding Principles and the Code on Interactions With Healthcare Professionals. However, this time, PhRMA should act BEFORE Congress or the FDA takes the first step!
What Do You Think?
The Regulation of Pharma Health Apps Survey asks whether or not you agree that it is in the drug industry’s best interest to police itself and develop best practices or self-regulatory guidelines for developing trustworthy health/medical apps for consumers and physicians.
It also asks if you agree or disagree with the following statements:
- Apps must include full disclosure regarding the company that has created the app or the sponsoring pharma company. This includes contact information.
BRANDED apps MUST include ISI (important safety information) up front in an easily accessible manner (e.g., on start-up screen).
- Apps that are BRANDED (i.e., mention drug brand names) must be available ONLY from the appropriate U.S. app site (e.g., Apple App Store) even if all the FDA-required ISI (important safety information) is included.
- Apps intended to be used by healthcare professionals in the U.S. must be HIPAA compliant.
- The pharmaceutical industry has to police itself with regard to development of all health apps regardless of what regulations FDA may impose.
- All health/medical apps should be certified by third parties such as Happtique.
- If an app relies on algorithms or formulas, it must be validated through rigorous testing and documentation to ensure it works properly (i.e,. calculations are correct).