This newsletter and reference library package will make sure you’re never at a loss when it comes to understanding what the regulators want from you.
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 monthly 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.
Your subscription also includes access to The Clinical Trials Advisor Regulatory Resource Center — a one-stop location for all the guidance, regulation and laws you’ll need to comply with U.S and international clinical trial requirements. The resource center will be updated continuously and available for you around the clock.
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