Integrated U.S. and
International Delivery
CEBIS combines leadership and clinical delivery with experienced international teams and qualified partners, aligning study planning and execution across countries with clear sponsor oversight and accountability.
Established Reach Across
CEBIS supports sponsors through established capabilities in the United States, Canada, Europe and India. Our teams and qualified partners work together to support clinical programs across study planning, operations, data, regulatory, safety, quality and related development functions.
United States
Established U.S. clinical development and operational capabilities.
Houston, Texas
Canada
Europe
Clinical development support across established European operations.
Switzerland · Romania · Ireland
India
Asia-Pacific
CEBIS is developing market opportunities and capabilities across selected Asia-Pacific regions.
These are future market development areas, not established CEBIS offices or current operational locations.
Coordinated Support
Across Regions.
Multi-country clinical development requires more than access to individual locations. CEBIS works to align study planning, operational execution and supporting functions across regions so sponsors maintain clear visibility and accountability throughout the program.
Support for Local and
Multi-Country Studies
CEBIS can support focused regional requirements or coordinate multiple functions across a broader clinical development program.
Single-Country Studies
Support tailored to the clinical, regulatory and operational requirements of an individual market.
Multi-Country Clinical Programs
Coordinated study planning and execution across multiple countries, sites and participating teams.
Central Oversight
Clear sponsor communication, study governance and program-level coordination across participating regions.
Local Execution
Regional clinical and operational capabilities aligned with the requirements of individual countries and study sites.
From Early Development Through
Post-Marketing Research
CEBIS supports clinical programs across Phase I through Phase IV, with capabilities that can be coordinated across established regions depending on the needs of the study.
Phase I & Early Development
Early clinical development, healthy-volunteer, patient, pharmacokinetic and specialized studies.
Phase II–III Clinical Development
Full-service clinical trial strategy, management, operational execution and data delivery.
Phase IV, Late Phase & Real-World Evidence
Post-marketing, observational, safety, outcomes and real-world evidence studies.
Consistent Oversight
Across Global Programs
Quality is integrated into study planning and delivery through controlled processes, independent oversight, risk-based review, audit programs, vendor qualification and inspection support.
CEBIS works to maintain clear study governance and sponsor visibility while coordinating activities across teams, sites, countries and qualified partners.
Quality Oversight
Structured processes supporting consistent study delivery.
Risk-Based Review
Identification and management of operational and study risks.
Vendor Qualification
Oversight of qualified partners supporting study activities.
Inspection Support
Preparation and coordination supporting inspection readiness.
Supporting International
Depending on the needs of the program, sponsors can engage CEBIS for individual services or coordinated support across multiple functions.
Planning a U.S. or International Clinical Program?
Tell us about your development phase, countries, study requirements and the support you need. A member of the CEBIS team will contact you to discuss the appropriate next steps.