Carolyn Troiano has more than 40 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco, e-cigarette/e-liquid and other FDA-regulated industries.
During her career, Carolyn worked directly, or on a consulting basis, for many of the larger pharmaceutical companies in the US and Europe, developing validation programs and strategies, and collaborated with FDA and other industry representatives on 21 CFR Part 11, the FDA’s electronic record/electronic signature regulation.
Carolyn Troiano has more than 40 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco, e-cigarette/e-liquid and other FDA-regulated industries.
The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability buil...
FDA has substantial authority to oversee regulated companies and their operations. The primary purpose of FDA is to assu...
The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability buil...
No advanced level courses available from Carolyn Troiano at the moment.
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