Brightech International
Everest Clinical Research is a full-service Contract Research Organization (CRO) built from a statistical and data management center of excellence. They provide a broad range of expertise-based clinical research services to the pharmaceutical, biotechnology, and medical device industries worldwide. Their foundation is built on biometrics services, and they have grown into a data and information-driven organization focused on quality and customer service. Everest serves some of the most well-known companies and works with advanced drugs, biologics, and medical devices in development today.
Industries
Nr. of Employees
small (1-50)
Brightech International
675 Cochrane Drive, East Tower, 4th Floor, Markham, Ontario, Canada L3R 0B8
Products
Clinical Data Dashboard
Web-based dashboard that centralizes clinical trial metrics and patient data from multiple sources (EDC, IWRS/IRT, eDiary/ePRO, CTMS) to provide visualizations, role-based access, downloadable listings, and near-real-time reporting.
Clinical Data Dashboard
Web-based dashboard that centralizes clinical trial metrics and patient data from multiple sources (EDC, IWRS/IRT, eDiary/ePRO, CTMS) to provide visualizations, role-based access, downloadable listings, and near-real-time reporting.
Services
Comprehensive biostatistics and programming services covering study design, statistical analysis planning, programming, and reporting for clinical studies.
EDC implementation, data cleaning, query management, dataset assembly and QC to support clinical trials.
Administration and data support for independent data monitoring committees including blinded/unblinded analyses.
Configuration and management of interactive response systems for randomization, drug supply, and patient-reported capture.
End-to-end project management, study start-up to close-out, resource planning and operational oversight for clinical programs.
Clinical safety case processing, periodic reporting, and safety analytics using enterprise safety database platforms and E2B workflows.
Comprehensive biostatistics and programming services covering study design, statistical analysis planning, programming, and reporting for clinical studies.
EDC implementation, data cleaning, query management, dataset assembly and QC to support clinical trials.
Administration and data support for independent data monitoring committees including blinded/unblinded analyses.
Configuration and management of interactive response systems for randomization, drug supply, and patient-reported capture.
End-to-end project management, study start-up to close-out, resource planning and operational oversight for clinical programs.
Clinical safety case processing, periodic reporting, and safety analytics using enterprise safety database platforms and E2B workflows.
Expertise Areas
- Biostatistics and statistical programming
- Clinical trial management
- Clinical data management
- Pharmacovigilance and drug safety
Key Technologies
- Electronic data capture (EDC) systems
- Interactive response technology (IRT/IWRS)
- eDiary / ePRO
- Clinical trial management systems (CTMS)