Looft, Fred J.
In order to ensure the safety and efficacy of post-market pharmaceutical products, the United States Food and Drug Administration relies on its pharmacovigilance efforts and input from the general public. The FDA receives submissions of adverse event reports from patients, health care practitioners and manufacturers. The FDA has started looking to the field of data mining to automate the search for safety signals. A training manual was created to introduce FDA employees to the concepts and applications of data mining techniques in pharmacovigilance.
Worcester Polytechnic Institute
Interactive Qualifying Project
All authors have granted to WPI a nonexclusive royalty-free license to distribute copies of the work, subject to other agreements. Copyright is held by the author or authors, with all rights reserved, unless otherwise noted.
Electrical and Computer Engineering
Your accessibility may vary due to other restrictions.