Our protocol optimization methodology translates your complex, scientific and regulatory document into a streamlined, interactive patient journey simulation, including site operational flow for your trial. We know optimization because we’ve guided hundreds of clinical studies through our proprietary process, identifying potential problems and helping sponsors drive quality from study start-up.
Our optimization methodology creates the foundation so:
- Your study team can see potential inconsistencies and implementation challenges.
- Your sites anticipate resource and operational requirements.
- Potential subjects envision the actual experience of participating.
- Regulators and ethics committees understand the complexities of the study design that can’t be fully appreciated through a static schema diagram.
