PSI CRO Expands Clinical Data Management Services To Offer Customers A More Secure Clinical Trial Environment

PSI CRO, a full-service Contract Research Organization, known for its time and money saving ability, by offering pharmaceutical sponsors delivery of clinical trials on-schedule and on-budget, announces recently successful expansion of its clinical data management services. In 2012, the scope of data management services provided by PSI using electronic data capture saw a significant increase over previous years. PSI’s data management teams have locked study databases for hundreds and thousands of patients, meeting predicted timelines and saving its customers months and years of time to market.

In response to the increasing needs of global clinical trials customers, PSI has broadened its clinical data management services to the UK, growing the team based out of Oxford. “We are pleased that the PSI Oxford office is growing in many dimensions – clinical, regulatory and now data management – all to align itself with our common goal: provide a safer and more secure clinical trial environment to our clients by running projects on-time and on-budget. This is PSI’s unique ability and we will do everything to keep and strengthen it,” said Sarah Eastty, Head of PSI UK.

About PSI CRO AG: 
PSI is a privately-held, full-service contract research organization (CRO), operating globally with 1,200 employees worldwide. PSI positions itself as a no-nonsense CRO capable of saving pharmaceutical sponsors millions of development dollars by consistently meeting clinical trial timelines. PSI’s global reach supports the operations of clinical trials across multiple continents and countries around the world.