Information Library
Results for: Brochures - Clinical Services - Phase I/IIa - Phase II/III
In the complex environment of the New Health, Quintiles is committed to helping you succeed. At every stage of your product’s lifecycle, we are dedicated to delivering real results, being proactive in navigating issues and thinking of new solutions. Search our library today.
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Accelerating Success in Oncology
March 9, 2012
New Demands to Demonstrate Value Require New Strategy Proof of efficacy is no longer enough to ensure success in oncology. As the cost and complexity -
A Focus on CNS
July 1, 2011
Quintiles is your ally for broad and deep CNS expertise in every aspect of the drug development process. -
Population PK/PD - Modeling and Simulation Optimization Tools
February 11, 2011
Population pharmacokinetic/ pharmacodynamic (PK/PD) modeling and simulation, available from Quintiles, is now endorsed by the FDA as often being instrumental in drug approval and labeling. -
The New Health Clinical Brochure
August 31, 2010
Japanese version available for download. -
Targeting Oncology
June 2, 2010
Learn more about Quintiles leadership in oncology product development and commercialization. -
Emerging Biopharma Service Fact Sheet
May 4, 2010
Recognizing that the needs of emerging companies are unique, Quintiles has created a specialized team dedicated exclusively to small and mid-sized biopharma companies. -
BIOS Standardize Data with SPARC
February 2, 2010
There is an increasing global requirement for Clinical Data Interchange Standards Consortium (CDISC) -based standardized data for regulatory submissions. At Quintiles, we have proactively addressed this need by training our staff, gaining experience, and developing and implementing innovative solutions for creating data that adhere to current CDISC Study Data Tabulation Model (SDTM) specifications. -
Validated Biomarker Menu
July 14, 2009
A comprehensive menu of validated cell, fluid and tissue based biomarker assays. -
Badania Kliniczne
April 10, 2009
Quintiles Poland świadczy usługi związane z organizacją i monitorowaniem Badań Klinicznych faz I-IV. Każdy nowy lek - zanim będzie dostępny w sprzedaży- musi przejść fazę wszechstronnych, specjalistycznych testów i uzyskać aprobatę organów rejestracyjnych.
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