A subscription to Clinical Trials Advisor (CTA) and will keep you up to date on the latest regulatory changes that govern drug and medical device clinical trials.
Clinical Trials Advisor helps clinical research sponsors and clinical sites researching drugs and medical devices gain new business, improve operations and keep in compliance with the FDA’s GCP requirements.
In addition to thorough analysis of regulatory developments, each biweekly issue highlights proven best practices for sites and sponsors, essential industry news, and tested techniques you can use to keep your clinical trials safe, compliant and efficient.
Each issue provides:
Plus, in every issue you get links to important documents from the FDA and international organizations, such as guidances, warning letters, Form 483s, and more.Bi-weekly, 30-day electronic trial subscription
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