Make better decisions, avoid FDA tangles, cut costs and boost trial success with Clinical Trials Advisor, the only independent, biweekly newsletter focused exclusively on clinical trial operations and good clinical practice compliance.
Every other week, you’ll get the latest clinical study news, as well as practical advice for maximizing your clinical investments. No other resource provides such valuable reporting and training applicable to every area of clinical trials. From ethics to information technology, training to patient recruitment, accreditation to disclosure — if it affects clinical trials, Clinical Trials Advisor covers it.
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Clinical Trials Advisor gives you the early warning on how your studies — and liabilities — are affected by developments not just from Congress and the FDA, but also from policymakers and regulators worldwide.
Plus, Clinical Trials Advisor is backed with a 100 percent money-back guarantee: If at any time you become dissatisfied, you may cancel your subscription and receive a refund of your subscription fee.
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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 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.
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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.
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