Full Service Solutions

Project management from start to finish.

Unlock your product's potential

Ready to go all the way? FSIHS’ Health Research Center can take your project from start to finish. Whether your end goal is FDA drug authorization, identification and substantiation of new structure and function claims, health claim substantiation, or enhanced scientific support, our team will manage the entire process for you.

End-to-end solutions alleviate the burden of IND management, regulatory approvals, protocol development, and implementation, providing you with a full service package.

Full Service Packages Include

Feasibility or Pilot Studies

Site Selection, Training, and Monitoring, if applicable

IND Complication & Submission

Clinical Trial Protocols

Participant Recruitment

Regulatory Document Management, Including Research Ethics

Clinical Trial Management and Execution

Data Collection and Biostatistics

Manuscripts for Submission to Peer Reviewed Journals

Clinical Trial Reporting

Results that make a difference

Some CROs provide simple cookie-cutter packages with general statistical reports. Our complete packages are developed with your end goal in mind, providing you user-friendly reports, submission ready documentation, and management of regulatory processes, where applicable.

Our team even compiles a research overview in lay terms for delivery to your entire team. Your sales department will love this user-friendly approach.

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