Our Scientific Affairs team plays a pivotal role in overseeing the integrity of the study process. With our expansive library of in-house data, our industry expertise and our experience working with global regulatory agencies, we develop study designs and project plans for regulatory markets around the world.
We also have a highly qualified team of full-time pharmacokineticists, biostatisticians, report writers, and protocol writers to ensure consistent quality and flexible turnaround times. As a client of PMRI, our technical expertise and unique insight is always at your disposal.
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