PHASTAR adds Data Management
By mutual agreement, PHASTAR are pleased to announce the acquisition of Exp-e-Data, an established provider of clinical data management services, to complement our current set of statistics, programming and medical writing offerings. PHASTAR and Exp-e-Data have successfully partnered on many projects for a number of years. Together, we can enhance the services to our customers due to the complementary nature of our companies, building on our shared philosophy, which is to ensure that the work we produce is of optimal quality: every project is supervised on methodology and utilises unique internal processes designed to ensure the highest standards.
The strong working relationships and team bonds forged between both companies over the years have led us to joining forces as a single company so we can grow in a seamless way whilst continuing to deliver a quality service that is ahead of our competitors.
Sheelagh Aird, CEO of Exp-e-Data will join the PHASTAR Management Team, adding her vast experience and knowledge of data management and the clinical trials process, to enable PHASTAR to offer a seamless service from data collection through to analysis, reporting and medical writing services. Together, we now have a strong team of technical statisticians, expert SAS programmers, meticulous data managers, clinical coders and medical writers, who combine to form industry leading project teams. Our teams have experience working on projects across all phases and therapeutic areas. Being a gold CDISC member, PHASTAR now has expertise across CDASH, SDTM and ADaM.
All staff are trained in the "PHASTAR Discipline" - our in-house approach to data collection and analysis. This comprises a set of common sense (but commonly ignored) principles developed by the PHASTAR management team based on observation and experience. The PHASTAR Discipline guarantees error-free results! PHASTAR teams can independently deliver standalone projects or partner with your company as a functional service provider, providing high calibre individuals with the ability to influence the direction of your clinical projects. We have a range of experience in different trial phases and therapeutic areas and can ensure that your trials have optimal designs and analysis methodology.