PROVEN SOLUTIONS

Effective, high-quality clinical trials require best-in-class, end-to-end solutions.

Take advantage of our years of experience and unique global network to comprehensively support your portfolio strategy, determine feasibility and rapidly develop sites in research-naïve areas.

WE ARE PROVEN

Conducting high-quality studies in challenging locations characterized by limited research/healthcare infrastructure, ongoing conflict and decentralized patient populations

Addressing challenges across dozens of therapeutic areas, including infectious diseases (IDs), neglected tropical diseases (NTDs) and emerging/reemerging diseases

Facilitating sustainable research capacity through training and by pairing sponsors with research-ready sites that have access to the right patient populations

Leverage our proven toolbox of resources for rapid study start-up.

Designed to support the entire study timeline, our resources have been developed and tested over our long history of conducting studies in challenging settings. These resources have been developed to aid with study start-up and conduct for sites with limited research experience.

Contracts
Templates and examples of contracts that span the typical study needs, including procuring supplies, consulting, laboratory services and more
Contracts
Standard operating procedures (SOPs)
Templates and examples of SOPs for studies of all types, including clinical trials, epidemiological studies and behavioral studies
Standard operating procedures (SOPs)
Checklists of key activities
Comprehensive lists of activities that should be completed during the study planning, start-up and conduct phases
Checklists of key activities
Plans
Templates and examples for monitoring, data management, statistical analysis, lab conduct and safety
Plans
Lists of organizational resources
Resources that assist with registering an in-country NGO, establishing a bank account, initiating payroll processes, procuring supplies and promptly paying vendors
Lists of organizational resources
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