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The company principals have 14 years of data management experience in a wide range of therapeutic areas in all four phases of clinical trials. We have managed and analyzed clinical studies ranging from small to complex Cancer trials to large global registration trials; in average of 3 years duration with several hundreds subjects.
Our goal is to provide our clients with data management, biostatistics and medical writing services that are secure,flexible and with leading-edge technology to complete their clinical studies quickly and cost-effective.
Our data management, biostatistics and medical writing services are governed by company strict SOPs and working practice and comply with ICH, CGP and GCP guidelines as well as FDA 21 CFR Part 11 regulations for electronic data capture.
Our expectation is to share the same commitment to innovation, professionalism and ethical standards. Our company will strive to build a reputation of quality, performance, experience and responsiveness to client needs, and to achieve the highest standards in the industry.
Hector Robertson, BS
Director, Data Management
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