Clinical Trials Advisor (CTA) is devoted to helping pharmaceutical
manufacturers, clinical researchers, IRBs and investigators improve clinical
trial operations and GCP compliance. You’ll get the latest regulatory and
international 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, CTA covers it.
Biweekly, 30-day electronic trial subscription
