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E-Consent in a Phase 1 Setting

Informed consent to participation in a clinical trial involves substantially more than obtaining signatures from subjects on a written form. It includes providing to potential participants enough information… Read more

Why use a Specialty Full Service CRO?

A common trend in the drug development industry is to utilize data and innovation to safely begin participant involvement earlier and earlier in clinical trials.¬† As innovation continues… Read more

Scientific Library

The directory provides a listing of our publications organized by area search, the year published or presented, and the type of publication such as a manuscript, meeting abstract, poster, etc. The publications are searchable by author, date, or keyword. The search results may take a minute to load so please be patient. Visit our Medical Communications service page for further information about our publishing capabilities.