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Tag Archives: drug development
Recap of the 20th CED Biotech/Life Sciences Conference
The 20th Annual Council for Entrepreneurial Development (CED) Biotech/Life Science Conference was held on 21-22 February 2011 in Raleigh, North Carolina. Continue reading
Posted in Conferences and Meetings, Industry News, Venture Capital
Tagged biotech, capi, Cato BioVentures, Cato Research, clinical research, conference, development plan, drug development, funding, healthcare reform, Phase 2, Phase 3, venture capital
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New Book – Principles of Anticancer Drug Development
Recently, Humana Press/Springer published a new book, Principles of Anticancer Drug Development. Neil Clendeninn M.D., Ph.D., a Senior Clinical Research Physician for Cato Research, served as an editor for the book, which has been described as a practical guide to the design, conduction, analysis and reporting of clinical trials with anticancer drugs. Continue reading
Posted in Publications
Tagged anticancer, cancer vaccine, Cato Research, clinical trials, drug development, FDA, pediatric, pharmacokinetics, preclinical, statistical analysis, toxicology, vaccines
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Electronic Data Capture Webinar with Merge Healthcare
Image via CrunchBase Electronic Data Capture (EDC) systems for clinical trials have been used for over two decades. For over 20 years, Merge Healthcare, a global healthcare IT company, has provided EDC solutions for clinical trials. Cato Research, an international … Continue reading
Posted in Clinical Trials, Webinars
Tagged Cato Research, clinical trials, CROs, drug development, EDC, Merge Healthcare, webinar
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Download the Slides from the Data Quality and Integrity Webinar
Yesterday’s free webinar, “Data Quality and Integrity: From Clinical Monitoring to Marketing Approval,” was a great success! For those who would like them, the slides from the presentation are now available for download here (PDF file). Stayed tuned Ask-Cato.com for … Continue reading
Posted in Clinical Trials, Regulatory Strategy, Webinars
Tagged Cato Research, clinical study report, clinical trials, data standards, drug development, marketing application, regulatory affairs, webinar
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Data Quality and Integrity: From Clinical Monitoring to Marketing Approval
At 2:00 PM ET on Thursday 18 November 2010, Cato Research will host a webinar titled, “Data Quality and Integrity: From Clinical Monitoring to Marketing Approval.” The webinar will be presented by Nancy Detich, Ph.D., a Senior Clinical Strategy Scientist … Continue reading
Posted in Clinical Trials, Regulatory Strategy, Webinars
Tagged Cato Research, clinical study report, clinical trials, data standards, drug development, marketing application, regulatory affairs, webinar
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