Integrated Clinical Research Solutions Across Phase I–IV
CEBIS is a full-service clinical research organization supporting Phase I–IV studies through integrated clinical operations, regulatory, data, statistical, safety, medical writing, quality and bioanalytical services.
A Sponsor-Focused CRO from Strategy Through Study Completion
CEBIS provides integrated clinical development support across the study lifecycle, from strategy, feasibility and start-up through clinical execution, data management, statistical analysis, medical writing and closeout. Our teams work as one coordinated organization to provide sponsors with clear accountability, responsive communication and reliable delivery.
Integrated Support Across Every Stage of Your Study
CEBIS brings together clinical, regulatory, data, statistical, safety, medical writing, quality and bioanalytical expertise to support sponsors from early planning through study completion.
Clinical Development Capabilities Built Around Sponsor Needs
Phase I–IV clinical trials
Bioavailability and bioequivalence studies
Specialized and complex study designs
Multi-site and multi-country clinical programs
Integrated clinical, data, statistical, safety and quality delivery
Bioanalytical support
Support Across the Clinical Development Lifecycle
CEBIS supports clinical development programs from early-stage studies through late-phase, post-marketing and real-world research.
Integrated Support for Bioavailability and Bioequivalence Studies
CEBIS supports bioavailability, bioequivalence and pharmacokinetic programs through coordinated clinical study execution and bioanalytical services.
BA/BE & Pharmacokinetic Studies
Preclinical Services & Specialized Testing
CEBIS USA manages and coordinates preclinical and specialized testing through qualified GLP facilities within its affiliate network. Services include preclinical studies, agrochemical testing, chemical testing, and GLP quality and compliance support.
Quality Embedded Across Every Study
Quality is integrated into study planning and delivery through controlled processes, independent oversight, risk-based review, audit programs, vendor qualification and inspection support. Our quality framework is designed to protect participants, preserve data integrity and support reliable regulatory submissions.
Controlled Processes
Defined procedures, documentation and responsibilities support consistent study execution across functions. Controls can be adapted to the needs, complexity and risk profile of the program.
Independent Oversight
Quality oversight provides a separate review perspective around study conduct, documentation, vendors and identified risks, supporting clear escalation and follow-through where issues are found.
Risk-Based Review
Review activities focus attention on critical processes, data and risks with the greatest potential impact on participant safety, data integrity, compliance and study delivery.
Audit & Inspection Support
Audit planning, readiness assessments, document review, team preparation and follow-up support help maintain inspection readiness throughout the study rather than only at the end.
Vendor Qualification
Third-party providers can be assessed and overseen against study requirements, quality expectations, assigned responsibilities and agreed performance or follow-up processes.
Experience Across Diverse Therapeutic Areas
CEBIS supports clinical development programs across a range of therapeutic areas and study types.
Experience Sponsors Can Build On
Experienced teams. Integrated delivery. Responsive sponsor support.
Explore Our Services
Clinical Development – Phase I to IV
Full-service clinical development from early-stage through late-phase and post-marketing research.
Bioavailability, Bioequivalence & Bioanalytical Services
Integrated BA/BE, pharmacokinetic and bioanalytical support.
Clinical Operations
Study execution, project management, site oversight, recruitment, supply and operational quality.
Data, Technology & Analytics
Data management, biostatistics, statistical programming and clinical technologies.
Regulatory, Medical Writing & Safety
Regulatory, writing, pharmacovigilance and medical oversight.
Preclinical Services & Specialized Testing
Coordinated preclinical and specialized testing through qualified GLP facilities within the affiliate network.
Clinical Research Professionals, Placed
Where You Need Them
Recruitment and placement of clinical research professionals for functional, temporary, project-based and permanent needs.
Ready to Discuss Your Study?
Tell us about your program and the support you require. A member of the CEBIS team will contact you to discuss the appropriate next steps.