FDA Looks Forward to Consumer Complaints to Rein In Supplements

FDA and FTC want consumers to help them find sellers of dietary supplements who make dubious claims or sub-standard products. Seems simple enough, but it is not. The agencies need stronger laws and additional resources to enforce the laws regarding supplements. Consumer complaints are not the answer. Dietary supplements account for about $100 billion sales … Read more

Coconut Had A Bad Week But We All Got A Lesson in Food Health Claims

This week the American Heart Association published a report rebuking coconut oil as one of the worst foods for heart health. The internet and new media used this report to thoroughly condemn coconut. Fair or not, this was a great learning moment for food manufacturers on changing fortunes linked to food health claims. The label … Read more

FDA’s Guidance Lists Best Practices For Using Electronic Systems in Clinical Trials     

This week FDA released a new guidance describing best practices for using electronic systems in regulated clinical trials and it all but confirms the already standard practice in the industry. However, the guidance will definitely help quality assurance and information technology personnel to enforce electronic hygiene. The guidance is organized in a Q&A format indicating … Read more

As Developers Push the Envelope with Smartphone Apps, FDA May Step Up too

Smartphone apps allow users to manage their own health and wellness; and FDA has taken a mostly hands off approach to regulating them. But with new apps being created to capture a variety of use and handling information to diagnose and potential help treat diseases, particularly neurological diseases, FDA may need to step in and … Read more

Medical Devices for Rare Diseases No Longer Need to Use Local IRBs

The Humanitarian Use Devices (HUD) form a small group of FDA regulated devices intended to treat rare disease. It is the device equivalent of the orphan drug designation for drug and biologics but much less popular than the orphan drug. There are only 63 HUD devices in the market; each year FDA approved 2-6 of … Read more

Google Search Trends And Personal Health Management  

What diseases people search for on the internet provides a useful hint to how that information is used. A list of 20 most searched diseases on Google is very surprising; it does not include any life-threatening disease and has a strange mix of indications seldom discussed together. But it points to an important trend. There … Read more

FDA is Very Worried Device Cybersecurity and So Should Be We

Last week FDA hosted its first conference on cybersecurity of medical devices where more than 100 experts discussed literally every aspect of the security of internet connected medical devices and healthcare delivery organizations (HOD), and the take home message was that medical devices are extremely prone to risk of hacking and there is long way … Read more

Fidget Spinner: Should FDA Regulate or Leave Them Alone?     

If you have young children, you must have a few spinning toys in your home, collectively called the “Fidget” spinners. The sellers of these seemingly innocuous “toys” make claims on their labels that should concern parents and regulators. But so far FDA has not shown any public desire to regulate these products. Fidget spinners are … Read more

Janet Woodcock Pulled a Frances Kelsey and Everyone is Mad

In FDA’s long and illustrious history, there are very few watershed moments that can be attributed to one person at the Agency. FDA historians consider the decision by Frances Kelsey to not approve thalidomide in 1960, despite extensive pressure to do so, as one of pivotal moments in its history that defined how it regulates … Read more