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PAREXEL Achieves 100th Asian Ethnobridging Study Milestone
Date:7/21/2011

tments to patients in Asia."

PAREXEL has enrolled over 3,500 subjects in Asian ethnobridging studies.  Early phase experts at PAREXEL conduct Asian ethnobridging studies at its accredited sites in the U.S. and UK.  These sites have access to an Asian population of over 1.2 million people, which allows PAREXEL to perform studies that conform to the regulatory requirements of China, Japan and Korea. PAREXEL experts have worked closely with Asian regulators to design studies, conducted outside of Asia for acceptance by the Asian regulators, that adhere to the International Conference on Harmonization (ICH) E5 guideline.  PAREXEL provides consultation on regulatory issues, protocol designs and analysis of data with relation to ethnobridging studies. The Company has a proprietary database and a dedicated enrollment team with experience in various specialized recruitment methods and access to some of the largest populations of first-generation Asians outside of Asia.

PAREXEL assists biopharmaceutical companies to manage development costs, accelerate development timelines and obtain earlier efficacy signals. PAREXEL accomplishes this by leveraging early phase capabilities that include a global capacity of  beds and full scope of early phase studies and services—from concept to study report and beyond, with integrated services to prepare clients for later phase studies. PAREXEL has extensive, relevant experience and in-depth expertise to assist clients with ever more complex early-phase trial design and execution, as well as efficient delivery of better, faster go/no-go decisions from First-in-Human (FIH) through Proof-of-Concept. PAREXEL provides specialized trial designs, state-of-the-art technologies, biomarkers, and scientific expertise. With hospital-based units in the U.S., Europe, and South Africa, as well as a network of alliance sites, PAREXEL provides
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