Clinical investigator fraud is a very real problem, and falls squarely within FDA\u27s mandate to protect the public health. The Eighth Circuit has held that under this mandate, FDA has the authority to impose affirmative duties to protect the public health by promulgating relevant regulations. FDA did promulgate such regulations, and the Eighth Circuit held that a failure to follow these regulations is a violation of section 355(i) of the FDCA. A violation of section 355(i) is considered a violation of section 331(e), and a violation of 331(e) can result in criminal sanctions under section 333(a). Thus, this tenuous chain of statutes allows the government to bring criminal charges against fraudulent criminal investigators. The Park Doctrin...
Fraud and misconduct in clinical research is widespread. Good clinical practice is a guideline adopt...
The pharmaceutical business is dominated largely by two types of entities: large, research-intensive...
Two sets of federal regulations, the Common Rule and Food and Drug Administration (FDA) regulation...
The number of clinical research investigators whom the Food and Drug Administration (FDA) has disqua...
Generalists daily make poor evidence-based decisions because regulatory and ethics committees fail t...
A letter report issued by the Government Accountability Office with an abstract that begins "The Foo...
In 2015, one of us published a peer-reviewed study, together with colleagues at the University of Ca...
This article criticizes the shift in focus from correction and compliance to punishment of pharmaceu...
Despite the imposition of increasingly substantial fines and recently successful efforts to impose i...
Professor Green addresses the matter of the proper balance between the tort system and regulation in...
There have been considerable charges and counter-charges the United States Food and Drug Administra...
Since Congress amended the False Claims Act (FCA) in 1986, the statute has evolved into a seemingly ...
Fraud is an increasingly expensive cost to the health care industry, and the regulatory and prosecut...
Publicly traded life science companies must navigate two overlapping regulatory agencies with distin...
This Article examines the interaction between direct regulation of pharmaceuticals under the Federal...
Fraud and misconduct in clinical research is widespread. Good clinical practice is a guideline adopt...
The pharmaceutical business is dominated largely by two types of entities: large, research-intensive...
Two sets of federal regulations, the Common Rule and Food and Drug Administration (FDA) regulation...
The number of clinical research investigators whom the Food and Drug Administration (FDA) has disqua...
Generalists daily make poor evidence-based decisions because regulatory and ethics committees fail t...
A letter report issued by the Government Accountability Office with an abstract that begins "The Foo...
In 2015, one of us published a peer-reviewed study, together with colleagues at the University of Ca...
This article criticizes the shift in focus from correction and compliance to punishment of pharmaceu...
Despite the imposition of increasingly substantial fines and recently successful efforts to impose i...
Professor Green addresses the matter of the proper balance between the tort system and regulation in...
There have been considerable charges and counter-charges the United States Food and Drug Administra...
Since Congress amended the False Claims Act (FCA) in 1986, the statute has evolved into a seemingly ...
Fraud is an increasingly expensive cost to the health care industry, and the regulatory and prosecut...
Publicly traded life science companies must navigate two overlapping regulatory agencies with distin...
This Article examines the interaction between direct regulation of pharmaceuticals under the Federal...
Fraud and misconduct in clinical research is widespread. Good clinical practice is a guideline adopt...
The pharmaceutical business is dominated largely by two types of entities: large, research-intensive...
Two sets of federal regulations, the Common Rule and Food and Drug Administration (FDA) regulation...