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Clinical Trials Advisor: Subscribe Now!

CTA SubscribeSubscribe to Clinical Trials Advisor (CTA) and keep up to date on the latest regulatory changes that govern drug and medical device clinical trials.

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:

  • Practical advice on maximizing your clinical investments
  • Updates on the latest regulatory and international news
  • Reporting and training applicable to clinical trials

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.

There’s absolutely no risk to you. You get our 100% Money-Back Guarantee: If at any time, for any reason, you become dissatisfied with Clinical Trials Advisor, you may cancel your subscription and receive a full refund. No questions asked.

So, why wait? Become a subscriber to Clinical Trials Advisor today. It couldn’t be easier.

Monthly, 12 issues/year