In Phase II-IV

PharmaNet offers all the clinical development services traditionally associated with conducting Phase II-IV programs. A key differentiating factor of PharmaNet is that in every program we conduct, PharmaNet provides an unrivaled combination of experienced project-management teams, senior management oversight, and an exclusive approach to building relationships with sponsors.
Protocol/Case Report Form Design

PharmaNet's experienced professionals apply their expertise to developing protocols and case report forms (CRFs) specifically for your clinical trials. Also, standardized CRF modules developed by PharmaNet are optimized for your trials to provide efficiencies in database design, edit checks, and tables and listings.

 

Additionally, protocol and case report form development capabilities include:

Relevant clinical/scientific considerations
Extensive feasibility
Determination of sample size
Statistical methodology
Design compliance with worldwide regulatory guidelines
Streamlined data collection
Systematic data recording that facilitates analysis
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