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Clinical Trials Advisor 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 impacts clinical trials, CTA covers it.
Biweekly, 24 issues
$550
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Published by ForeSite Publishing, Inc., ForeWard is the first newsletter specially customized for your research site, containing information about your studies and your research practice. Today achieving your enrollment goals is one of the biggest challenges in conducting clinical research. After receiving just three issues of ForeWard, readers surveyed show a remarkable trend: Their willingness to participate in clinical research increased by 50%. Think of how that can positively impact your enrollment efforts!
Quarterly, 4 issues
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Each Wednesday morning turn to RxTrials Institute Drug Pipeline Alert for the latest intelligence on the research and development of new drugs in high-cost therapeutic areas such as oncology/hematology, cardiovascular, pediatrics, respiratory and others. Issues cover U.S. and international clinical trials, medical research, drug applications and co-development activities. Sign up today to start receiving RxTrials Institute Drug Pipeline Alert.
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Clinical Trials Indemnification Clauses: Pitfalls and Problems to Avoid is the management report that examines the most problematic areas in negotiating indemnification clauses. This report highlights the key topics you need to address and provides insight into the types of agreements that are generally accepted standards in the industry.
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Clinical Trial Inspections: How to Prevent a Bad Outcome is brought to you by RxTrials Institute. Discover how to confidently navigate the FDA’s inspectional process: before, during and after a GCP inspection. Use the clinical trial compliance tool created by a former FDA inspector, customize an auditing checklist and capture your most critical endpoint data, and put best practices to work when auditing and training your research staff.
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