Date :
Place : United States, Littleton
Website :https://globalwizdom.com/product/7235
Contact Person:Michael Smith
Description:
We will discuss the importance of applying industry best practices when testing the IT system used in an FDA-regulated environmentDeadline for abstracts/proposals : 7th April 2020
Organized By :Global Wizdom
Keynote Speakers : Carolyn Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device, and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs.
Conference Highlights :This course will describe the best practices for testing, including “who” should be responsible for tasks, “how” the testing should be accomplished, and “what” specific criteria will be used to define acceptance. FDA guidelines are very specific in terms of how this is to be done.
Check the event website for more details.