SERVICES OVERVIEW
WHERE REGULATORY EXPERTISE MEETS CLINICAL PRECISION
SERVICES OVERVIEW
WHERE REGULATORY EXPERTISE MEETS CLINICAL PRECISION
Functional Service Provider To Full-Service CRO
LBRIA is a full-service CRO supporting the clinical development lifecycle from IND submissions and early-stage development through approval and post-marketing activities. LBRIA has successfully rescued all phases of Clinical Trials. Our services are fully modular, allowing sponsors to engage LBRIA for end-to-end program delivery or to select individual functional services that integrate seamlessly with your existing teams.
LBRIA understands early stage development is lean, and we provide a risk-aware approach that combines scientific and regulatory guidance to support efficient protocol design and study conduct. We maintain transparency in pricing, providing sponsors with clear visibility into scope, timelines, and costs—while retaining the flexibility to scale support as programs evolve.
LBRIA’s Flexible & Scalable CRO Services
Whether you need support for a specific study component or a full-service partner from early development through FDA submission, our services scale to your program’s needs.
Select a service below to find out more.
