Study Start-Up

The key to swift clinical trial start-up is a combination of efficient regulatory submission and approval, as well as expedited investigator site activation. Reducing the cycle time of study start-up requires strong therapeutic expertise, a focus on working with sites proactively during start-up, a profound understanding of dynamic global and local guidelines, and a broad geographic network of regulatory personnel. Drawing on extensive clinical research expertise and site knowledge, our teams work in tandem with yours to efficiently manage every aspect of study start-up.

Why ClinChoice for Study Start-Up?

Bring your research to life with ClinChoice’s comprehensive package, encompassing regulatory expertise and team capabilities to ensure the overall success of your study.

Robust regulatory expertise spanning local laws and global guidelines

Dedicated project team members to streamline and optimize every facet of study start-up

Project management grounded in quality, risk mitigation, cost-effectiveness, and precise timing

Proactive and detailed communication and planning with our clients

Study Start-Up Services

Start-up differs in every study. Our services apply across diverse sectors, each with unique considerations.

For Pharma & Biotech

Applying regulatory and clinical expertise, as well as our global reach and established site network, to optimize start-up times and initial planning phases.

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