STATISTICAL SERVICES Clinical Trial Statistics are an integral part of any efďŹ cient clinical trial study. PSI clinical trial statisticians are experienced in working with our clients to design their clinical trial, determine endpoints, provide statistical methods and sample size determinations, as well as provide quality data oversight during the program. PSI Clinical Trial Statistics Department The PSI Director of Statistics has 18 years of experience in the pharmaceutical industry PSI statisticians and SAS Programmers have an average of over seven years in the industry Industry experience and depth of knowledge allow the PSI statistics department to deliver quality results on-time PSI Biometrics Group has experience of placebo-controlled Phase II-IV clinical trials, observational studies, non-interventional studies/scientiďŹ c programs and full integrated analyses of programs. Our stats group has diverse experience in generating Statistical Analysis Plans, Final/Interim Analyses Reports, ISS/ISE Summaries, Annual Reports and Safety Reviews for DSMBs. They also support the compilation of Clinical Trial Reports and Manuscripts.
PSI CRO AG Corporate Headquarters Baarerstrasse 113a 6300 Zug, Switzerland Tel: +41 41 228 10 00
Global Office Locations North America Ft. Washington, PA Burlingame, CA San Francisco, CA
Latin America Buenos Aires, Argentina
Europe Oxford, UK Munich, Germany Neusiedl am See, Austria Minsk, Belarus Sofia, Bulgaria Prague, Czech Republic Tallinn, Estonia Budapest, Hungary Milan, Italy Warsaw, Poland Bucharest, Romania Belgrade, Serbia Kiev, Ukraine Russian Federation: St. Petersburg, Moscow, Novosibirsk
Operational Presence by Region North America / Europe / Latin America Asia-Pacific / South Africa
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