Comprehensive Clinical Trial ServicesRanging from study startup through FDA submission
Study start up
Ongoing study management
Multi-vendor management (central lab, drug supply, IRB)
Site monitoring (site selection, initiation, interim, close-out)
Study rescue/cleanup
Site and monitor training & auditing
Data management*
Statistics and medical writing*
FDA submissions*
*Partner Company
Customized Services
Only need to outsource a portion of your study? Our “a la carte” approach to trial management allows you to choose the services you need for your study at any level—from overall project management to site management or monitoring only. We offer you this flexibility while always ensuring the highest quality management services.
Monitoring Only
We will form a team of monitors and manage them at a much lower cost than most staffing agencies or large CROs.
Study Management Only
We will assign an experienced Study Manager to manage your study and vendors including a large CRO.
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