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About us
Chairman Message
Board of Directors
CEBIS Team
Mission & Vision
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R&D – Pre-Clinical Testing
Discovery Toxicology
Agro-chemical & Chemical Testing
Biocompatibility Testing
Diet Formulation
Batch Release Test
Clinical Research
Drugs & Biologics
From Idea to Market
Phase I-IV Clinical Trials
PMOS
Disease Registries
Regulatory Affairs
Regulatory Management
CTD for Drugs
European Registration Procedures
Marketing Authorization Maintenance
Clinical Trial Applications
Our Expertise
Medical Devices
Development
Pre-CE Mark Lab Studies
Clinical Evaluation
MDR Technical Documentation
MDR Rationale Classification
PMCF
Dietary Supplements & FSMP
Development
Safety & Efficacy Clinical Trial
Regulatory Affairs
BA/BE Studies
Bio-Analytical Services
Supplies & Logistic
Clinical Supply Management
Clinical Trial Supply Services
Global Logistics Management
TRIAL MATERIALS LABELLING & PACKAGING
Cold Chain Storage & Delivery
Temperature Controlled Packaging
IRT, EDC & Biostatistics
Interactive Web Response System (IRT/IWRS)
EDC/eCRF
Clinical Trial Management (CTM)
Trial Planning and Analytics solution
Data Management & Biostatistics
Global Research Centers
Research Sites Network
Patient Recruitment, Retention, Engagement
Facilities
Laboratory
Drug & Device Safety
Global PV HUB
Key Points
How can we Help?
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Outsourcing PV
Multiple Competitive Advantages
for Study Development
Availability of Rescue Countries
& Clinical Research Sites
High competitive advantages
with a focus on patients' safety
Integrated Software solutions for all phases
of clinical research, RWE, Device studies.
GLP Accredited Pre-Clinical and Clinical
facilities in North America, Europe and India
Interoperable, Flexible and Reliable
processes with Global Compliances
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RFP-RFI
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Training & Staffing
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Home
RFP-RFI
Careers
Training & Staffing
Investigators
Resource Centre
Contact
About us
Chairman Message
Board of Directors
CEBIS Team
Mission & Vision
Ways We Work
Business Ethics
R&D – Pre-Clinical Testing
Discovery Toxicology
Agro-chemical & Chemical Testing
Biocompatibility Testing
Diet Formulation
Batch Release Test
Clinical Research
Drugs & Biologics
From Idea to Market
Phase I-IV Clinical Trials
PMOS
Disease Registries
Regulatory Affairs
Regulatory Management
CTD for Drugs
European Registration Procedures
Marketing Authorization Maintenance
Clinical Trial Applications
Our Expertise
Medical Devices
Development
Pre-CE Mark Lab Studies
Clinical Evaluation
MDR Technical Documentation
MDR Rationale Classification
PMCF
Dietary Supplements & FSMP
Development
Safety & Efficacy Clinical Trial
Regulatory Affairs
BA/BE Studies
Bio-Analytical Services
Supplies & Logistic
Clinical Supply Management
Clinical Trial Supply Services
Global Logistics Management
TRIAL MATERIALS LABELLING & PACKAGING
Cold Chain Storage & Delivery
Temperature Controlled Packaging
IRT, EDC & Biostatistics
Interactive Web Response System (IRT/IWRS)
EDC/eCRF
Clinical Trial Management (CTM)
Trial Planning and Analytics solution
Data Management & Biostatistics
Global Research Centers
Research Sites Network
Patient Recruitment, Retention, Engagement
Facilities
Laboratory
Drug & Device Safety
Global PV HUB
Key Points
How can we Help?
Our Solutions
Resources
Outsourcing PV
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CEBIS USA
CEBIS Inc. – USA
7080, Southwest Fwy,
Houston, Texas – 77074