ResearchPoint excels in managing the entire clinical trial process and producing consistent, quality data. Our cross-trained team of seasoned professionals provides customized management of the clinical development process, reducing time, risk and cost for our customers.

Project Management Data Management Clinical Monitoring Safety Monitoring Regulatory Support Quality Assurance Support Quality Control Protocol Consulting & Design

Site Selection Site Management Cardiovascular Safety & Diagnosis Services Medical Writing Biostatistics Online Training Online Investigators' Meeting Online Technology Collaboration (ClinPOINT©)

Our Continuum Business Model = Value-Added Outsourcing Experience

	Streamlined management process versus the typical silo infrastructure
	Cross-trained teams
	Integrated monitoring and data management functions
	Constant, efficient flow of communication with customers and project team

Our Data Services = Cost & Time Savings

Data solutions for early- and late-phase clinical trials, using conventional paper case report forms or electronic data capture (EDC).

ClinPlus® Data Management (CPDM) provides the means to achieve efficient data processing with minimum setup time. CPDM includes an array of features that facilitate page, record, and query tracking; review cleanup cycles; medical coding; complete audit trail maintenance and role-based security. By managing clinical data management with one system, customers are ensured a smooth progression from entry of first casebook to a clean and locked database. Data are entered directly into SAS® native data sets so information is instantly accessible for analysis.

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