Design an optimal schedule of trial activities to accurately predict and heighten study performance.

• Better evaluate protocol design and reduce risk of costly amendments.

• Create and compare multiple scenarios and model cost tradeoffs, reducing risk and expenditures, improving the site and patient experience and decreasing study timelines.

• Simplify the schedule of activities by identifying and removing unnecessary trial procedures and visits.

• Reduce site and patient burden by highlighting and eliminating barriers to participation and satisfaction.

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Tap into our clean, multi-sourced, easily searchable global data repository optimize study planning and better match investigators and sites to trial objectives.

• World’s largest and most up-to-date historical performance and Site repository.

• Results in smarter list of sites built on an integrated view that reduces time/costs of selecting sites, avoids/minimizes non-performing sites and increases investigator engagement.

• Inter-company and sponsor/CRO data sharing arrangements possible for heightened performance.

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More predictably plan, manage, and flexibly re-forecast patient enrollment scenarios

• Designed to handle study complexities and multiple operating models.

• Shortens timelines and optimizes operational execution.

• Pressure tests CRO bids to validate enrollment feasibility.

• Keeps you on top of study enrollment progress via real-time data feeds.

• Provides early insights into potential risks or delays; enables rescue strategy modeling.

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Employ strategic, data-driven feasibility regarding trial strategy and planning, protocol finalization, and selection of the most appropriate countries and sites.

• Drives proven, accelerated results due to fit-for-purpose technology and automation.

• Improves country and target site identification and information gathering.

  • Streamlines CDA negotiations

  • Drives faster survey completion and site selection process

• Heightens investigator experience and loyalty.

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Efficiently, accurately and confidently budget across all trial phases, indications and countries

• Employ the industry’s largest, most efficient and accurate clinical budgeting tool Leverage line-item costs at fair market value to accurately build and adjust study budgets and boost compliance.

• Leverage line-item costs at fair market value to accurately build and adjust study budgets and boost compliance.

• Streamline, simplify and accelerate investigator negotiations.

• Up-to-date information is continuously expanded and refreshed quarterly.

• Standard of Care module helps avoid supplicate spending on insurance-covered procedures. View previously agreed site-level budget iterations.

• Also available: GrantPlan for Investigator-initiated Studies (GPI), the only tool built specifically for investigator-initiated studies.

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