Protocol/Case Report Form Design

Optimized efficiencies. Compliant designs.

A protocol or case report form (CRF) that’s vague, confusing, or incomplete could cause delays, unnecessary expenses and compromised data. PharmaNet/i3 professionals are highly skilled in developing protocols and CRFs, including electronic versions, specifically for your clinical trials, optimized to provide efficiencies in database design, data collection, edit checks, tables, and listings.

Additionally, protocol and CRF development capabilities include:

• Relevant clinical/scientific considerations
• Determination of sample size
• Statistical methodology
• Compliance with worldwide regulatory guidelines
• Streamlined data collection strategies