Subscribe to Clinical Trials Advisor (CTA) the only newsletter designed especially for the clinical trials professional charged with gathering submission-quality data while protecting the safety and welfare of study subjects.
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.
Each issue of Clinical Trials Advisor provides :
- Proven best practices to improve operations for sites and sponsors
- Essential industry news, including international news, to keep you fully compliant.
- Tested techniques to keep your clinical trials safe, compliant and efficient
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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Monthly, 12 issues/year. Electronic Delivery.