CEBIS
Global full-service contract research organization providing clinical development, regulatory, pharmacovigilance, medical device support, bioanalytical and supply-chain services across North America, Europe and India. Offers GLP-accredited preclinical and clinical facilities, PV hub operations, integrated software-enabled clinical processes, and ISO-certified management systems to support drug, biologic, device and nutraceutical development from concept to market.
Industries
Nr. of Employees
medium (51-250)
CEBIS
Products
Electronic Data Capture (EDC) and eCRF Management
A web-based system for designing case report forms, capturing clinical trial data, and managing data quality through validation and query management.
Global Pharmacovigilance Hub (Global PV HUB)
A service platform for managing drug and device safety monitoring and reporting on a global scale.
Clinical Research Services
Comprehensive clinical trial services including drug, biologics, medical devices, dietary supplements, bioanalytical, and pharmacokinetic/pharmacodynamic studies.
Clinical Supply Management and Interactive Web Response System (IWRS)
Management of clinical trial supplies including sourcing, packaging, shipment, storage, and subject randomization via an interactive web system.
Trial Materials Labelling and Packaging
Services for designing, printing, packaging, and labelling clinical trial materials compliant with regulatory standards, including cold chain and on-demand packaging.
Research Sites Network
A network of over 300 clinical research sites across North America, Europe, and India for site feasibility, selection, and trial execution.
Electronic Data Capture (EDC) and eCRF Management
A web-based system for designing case report forms, capturing clinical trial data, and managing data quality through validation and query management.
Global Pharmacovigilance Hub (Global PV HUB)
A service platform for managing drug and device safety monitoring and reporting on a global scale.
Clinical Research Services
Comprehensive clinical trial services including drug, biologics, medical devices, dietary supplements, bioanalytical, and pharmacokinetic/pharmacodynamic studies.
Clinical Supply Management and Interactive Web Response System (IWRS)
Management of clinical trial supplies including sourcing, packaging, shipment, storage, and subject randomization via an interactive web system.
Trial Materials Labelling and Packaging
Services for designing, printing, packaging, and labelling clinical trial materials compliant with regulatory standards, including cold chain and on-demand packaging.
Research Sites Network
A network of over 300 clinical research sites across North America, Europe, and India for site feasibility, selection, and trial execution.
Services
Protocol development, regulatory/ethics submissions, site selection and monitoring, project management, data management and study close-out for Phase I–IV studies.
Safety case intake, coding, causality assessment, timely regulatory reporting, PV training, PSMF maintenance, RMP/RMM support and QPPV outsourcing.
Pre-CE mark lab studies, clinical evaluation reports, MDR technical documentation, classification rationale and post-market follow-up studies.
Design and conduct of PMOS and disease registries to generate real-world evidence and epidemiological metrics across multiple therapeutic areas.
Bioanalytical testing, BA/BE studies and PK-PD analyses to support early and later-phase clinical programs.
Sourcing comparators, manufacturing investigational products/placebos, import/export management, storage and global distribution for clinical trials.
Protocol development, regulatory/ethics submissions, site selection and monitoring, project management, data management and study close-out for Phase I–IV studies.
Safety case intake, coding, causality assessment, timely regulatory reporting, PV training, PSMF maintenance, RMP/RMM support and QPPV outsourcing.
Pre-CE mark lab studies, clinical evaluation reports, MDR technical documentation, classification rationale and post-market follow-up studies.
Design and conduct of PMOS and disease registries to generate real-world evidence and epidemiological metrics across multiple therapeutic areas.
Bioanalytical testing, BA/BE studies and PK-PD analyses to support early and later-phase clinical programs.
Sourcing comparators, manufacturing investigational products/placebos, import/export management, storage and global distribution for clinical trials.
Expertise Areas
- Clinical trial management
- Pharmacovigilance and drug/device safety
- Medical device regulatory and clinical evaluation
- Bioanalytical and PK/PD services
Key Technologies
- Regulatory adverse-event reporting systems
- Safety database and signal detection platforms
- AI-driven clinical trial modeling and simulation
- Risk-based monitoring tools