Subscribe to Clinical Trials Advisor (CTA) and keep 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 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:
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
BONUS: Subscribe to Clinical Trials Advisor NOW and save $100 off the regular one-year price of $645 — plus receive a FREE copy of our webinar CD, Best Practices for Managing Clinical Trial Materials – a $347 value!
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. Electronic Delivery
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