No matter how bad things seem for the United States Food and Drug Administration these days, 20 years ago they were arguably worse. In the late 1980s, the agency was embroiled in a generic-drug scandal, in which FDA administrators accepted bribes for quick drug approvals, and drug makers admitted to deliberately defrauding drug regulators. The days when the federal agency could rely solely on the trustworthiness of the industry it was supposed to be regulating were done.
But from the ashes of the generic-drug scandal, some positives did arise. One of the programs resulting from the scandal, and the subsequent Generic Drug Enforcement Act of 1992, was the FDA’s mission to “debar” people or whole companies from participation in agency activities, such as applying for drug approval, if found guilty of deliberate fraud.
David Read, who was the FDA’s first Debarment Task Force chair, says that when the agency first set out to ban investigators for fraudulent activities involved with the generic-drug scandal, the magnitude of dishonesty in the drug business was staggering. “[The Generic Drug Enforcement Act] resulted in a lot of investigations, which turned up a lot of surprises,” he says. “As people started investigations, they found things that weren’t expected….”
Biotech Ethics BLOG
This blog is about ethical issues in the biotechnology industry. That includes all 3 main areas of that industry: health biotech, food biotech, and industrial biotech. (The last two are particularly important, and don't get enough attention.)
Unlike my Business Ethics Blog, this one will focus on aggregating information, rather than offering much commentary.
The Business Ethics Blog (by Chris MacDonald)
The Research Ethics Blog (by Nancy Walton and Chris MacDonald)
Genethics.ca (by Bryn Williams-Jones)
Ethics of Complementary & Alternative Medicine
Pages on this Site:
Ethics for the Biotech Industry (my scholarly research)