FDA Prescription Drug Expert
Prescription drugs play an enormous role in medicine and clinical settings today, which is why medical law is so extremely complex.
The number of drugs on the market complicated by drug-to-drug interactions, pharmacological mechanisms of action, complex pharmacokinetics, and narrow therapeutic windows can cause unpredictable safety situations in clinical settings.
The complexity of it all can be overwhelming to even the experienced physician, pharmacist or scientist.
For this reason, the input from a drug expert can be informative, especially regarding medical law and FDA regulation, as the Food and Drug Administration is literally the most regulated industry in the entire world. Ideally, when bringing a drug expert into a case, you want them be experienced in all aspects of drug use and clinical trials and testing prior it is approval, and well versed with FDA law.
Whether for a deposition or tesitmony, having a former FDA drug expert as your expert witness and consultant will make all the difference.
This includes drug development, the clinical use of drugs, and the federal regulation surrounding drug development and the clinical use of drugs.
A drug expert would have to have direct experience working in running clinical trials, from both a federal/regulatory standpoint, from an academic institution standpoint, as well as from a pharmaceutical industry standpoint. In addition to a complete scientific knowledge, the drug expert would need to be familiar with the clinical use of drugs and epidemiology thereof.
Contact an experienced prescription drug expert here.