"One of the major challenges for rare disease clinical research is that increasingly innovative products are evaluated within limited patient populations with refined phenotypes and significant unmet needs. In this setting, traditional methods of program design may be ill-suited in scope and timing to address the spectrum of questions defining clinical utility as well as product value," said Dr. Murphy. "During this webinar we'll examine the impetus for innovation and the impact of observational research techniques as companion initiatives informing patient access."
Dr. Murphy will be joined by several of his Worldwide colleagues who will bring their expertise to the discussion, including Josie Measures, Vice President of Biostatistical Operations; Lorna Graham, Associate Director, Project Management, Evidence; and Barbara Zupancic, Director, Global Patient Recruitment and Retention.
To register for this free Worldwide Clinical Trials webinar, visit: https://www.worldwide.com/observational-research-orphan-drug-development-webinar/
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About Worldwide Clinical Trials
Worldwide Clinical Trials employs more than 1,400 professionals around the world, with offices in North and South America, Eastern and Western Europe, Russia and Asia. One of the world's leading, full-service contract research organizations (CROs), we partner with sponsors in the pharmaceutical and biotechnology industries to deliver fully integrated clinical development and bioanalytical services, extending from first-in-human through phase IV studies. Grounded in medicine and science, we help sponsors move from medical discovery into clinical development and commercialization across a range of therapeutic areas, including neuroscience, cardiovascular diseases, immune-mediated inflammatory disorders (IMID), and rare diseases. For more information, visit http://www.Worldwide.com.
SOURCE Worldwide Clinical Trials