VIDEO LIBRARY

Presented at Medidata NEXT 2022 in New York City.

PROMETRIKA’s Chelsey Ryan, Associate Director of Clinical Operations and Pharmacovigilance, speaks at the Chief Medical Officer Summit 360°

Chelsey Ryan, Senior Clinical Trial Manager, PROMETRIKA, LLC joined this MassBio panel discussion on the imperative that clinical trial sponsors embrace technical innovation to meet the demands of today’s world. This forum focused on how tools such as eSource and Direct Data Capture help trialists make confident, informed decisions, ensuring certainty of data from initial collection to regulatory submission.

As a full-service CRO at the heart of drug development, PROMETRIKA has witnessed the increasingly rapid shift toward remote medicine and the impact this has on clinical trials. On the leading end of this spectrum is the push toward de-centralized clinical trials (DCT) that promises many benefits in costs, patient inclusion, and execution of clinical trials.

In a global drug development landscape, many biotechs face significant challenges: varying regulatory regimes, local site infrastructure, supply chain logistics, language barriers, and consistency of data integrity across regions. PROMETRIKA hosted a webinar diving into how a region-specialized, global partnership of CROs can help you overcome these complexities – without sacrificing quality or control.