FDA additions to Informed Consent – Will they help improve participant engagement?
By Paul Ivsin, Executive Vice President, Analytics, Insights, and Media If there is one thing we can agree on, it’s that informed consent forms (ICFs) for
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1. National Academy of Sciences. The Prevention and Treatment of Missing Data in Clinical Trials. Washington, D.C.: National Academies Press; 2010. Available at: www.nap.org.
By Paul Ivsin, Executive Vice President, Analytics, Insights, and Media If there is one thing we can agree on, it’s that informed consent forms (ICFs) for
Combined businesses unlock significant opportunity for clients with strategic, differentiated clinical trial recruitment, engagement and retention approaches, along with compelling creative solutions and best-in-class analytics.
Earlier this month, leaders at Continuum Clinical gained valuable insight into upcoming trends in clinical research, study sites, digital health, and the convergence of healthcare
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