for Clinical Trials
ClinBAY is a global biometrics CRO with headquarters in Cyprus, Europe. Our services involve statistical consulting and programming on clinical trials, functional sourcing and software development.
Top Biometrics Services
Our services involve statistical consulting and programming on clinical trials. We manage approximately 40 clinical trials per year, spanning from phase I to phase IV. Our consultants are also available for functional sourcing support in Biometry. Last, we develop custom data analysis packages in R and SAS.
Statistical Consulting
Our statistical experts help you to reduce clinical development costs and expedite drug approvals using innovative study designs and cutting-edge statistical techniques.
Analysis and Reporting
We are a reliable and cost-effective partner for the analysis and reporting of your clinical trials. From protocol to SAP, our core services also include production of high-quality ADaM data and TFL with SAS.
Functional Sourcing
You are looking for a contractor for a near-term assignment? We can set up a dedicated team of qualified statistical and programming consultants that would suit your needs. Contact us to check current availabilities
Software Development
We develop custom R packages, SAS macro libraries, and software packages to automate the display, processing and analysis of data. See some recent examples here.
Do you want to produce a data listing in less than 30 seconds? Check out our ClinXPORT software to streamline and automate trial reporting activities!
Why Choose Our CRO?
Do you want a statistical partner that is reliable and independent, experienced in over 300 clinical trials and working in business since more than 10 years? Get in touch with us, to take the next step in ensuring your study is successful.
Our Goal
To become and remain your preferred CRO biometrics partner for clinical trials
We help you to design a cost-effective trial to validate your study objectives.
We streamline the analysis and reporting of your study, providing decision-enabling results in record time, with no issues.
We help you to take the best decision for your drug, at the study and program level. We assist you in combining data across trials and in scientific communications about your product.
We provide expert regulatory statistics support for EMA, FDA and global marketing authorizations. We build strong statistical dossier and facilitate regulatory interactions for a fast-track approval.
We will be pleased to hear about your trial project and provide you with a tailored-made, cost effective biometrics solution.
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