By Dr Nicola Davies
The US Food and Drug Administration strictly prohibits the distribution of counterfeit, diverted, subpotent, substandard, adulterated, misbranded, and expired drugs that pose a serious threat to life. Nevertheless, such drugs continue to end up in circulation, compromising patient safety.
The Office of Criminal Investigations (OCI) is responsible for all FDA-conducted investigations, including those on suspected illegitimate drugs. Additionally, it participates in several law enforcement task forces, with the FDA sometimes coordinating with the Federal Bureau of Investigation (FBI), United States Department of Agriculture (USDA), and other agencies in the enforcement of drug distribution laws.1
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze