Spiderman is Real! Well.. May be Soon

Not really, but we might be going down the road to create one with NIH funding. This week, NIH lifted a moratorium on insertion of human stem cells into early stage embryos of non-human vertebrate animals to create human-animal chimera. This represents a unique balance of scientific curiosity, medical benefit, and ethical dilemma. Human-animal chimeras have dominated … Read more

Want to Make Wearable Devices More Appealing? Register with FDA

This week Philips Healthcare announced release of a smart watch very similar in functionality and appearance to Fitbit, Apple’s iWatch or Samsung Gear watch. However, the Philips watch has one difference from its competition; it is registered with the FDA as a medical device. Smart watches are not considered medical devices by FDA and do not require registration or … Read more

Email Leaks, Politics and FDA-Regulated Industry

An email leak from a Democratic National Committee (DNC) led to the Chair of the DNC losing her job and the leader of the party barely surviving a major crisis on the eve of the convention. This followed concerns of security of personal and official emails. This episode highlights once again the high-risk of electronic … Read more

Manufacturers of Biologics to Increasingly Use Single-Use Technologies

Biologics manufacturing facilities using traditional stainless-steel bioreactors have to deal with significant manufacturing suite unavailability between production cycles due to expensive cleaning technology, extensive cleaning validation, and the associated loss of productivity and revenue. The use of single-use and disposal technologies such as single-use bioreactors (SUB) can greatly increase the production efficiency by reducing the … Read more

FDA Clarifies: You Cannot Compound Approved Drugs

Last year, during the drug pricing debate triggered by Turing Pharma’s Martin Shkreli, a San Diego compounding pharmacy Imprimis Pharmaceuticals announced that it would offer a cheap compounded version of the expensive FDA-approved drug. At that time, we criticized Imprimis based on our belief that such a practice will jeopardize all approved drugs. This week FDA confirmed … Read more

Gifts to FDA: FDA’s Strangest Guidance Document

A new draft Guidance Document on “Gifts to FDA” could be one of the strangest documents of its kind released by the Agency in its history. The document defines a “gift” to the FDA and then details the various rules that would govern the evaluation and acceptance of such gifts. Only the FDA Commissioner is … Read more

FDA User Fee for OTC Drugs: Beware of What You Wish For.

Last month, FDA held a public hearing to collect public opinions about enacting a new user fee for over-the-counter (OTC) drugs. The presenters at the hearing could be divided into three groups with distinct preferences. The FDA was the host of the hearing and a strong proponent of the OTC user fee giving several reasons why a user fee … Read more