Everest Clinical Research
Everest Clinical Research is a full-service contract research organization (CRO) dedicated to providing a broad range of expertise-based clinical research services to the pharmaceutical, biotechnology, and medical device industries worldwide. With a foundation built on excellence in biometrics, data management, and clinical trial services, Everest aims to deliver high-quality, customer-focused solutions to support the development of advanced drugs, biologics, and medical devices. The company emphasizes quality, innovation, and a can-do culture, operating globally with offices in North America, Europe, and Asia, and serving over 100 active clients.
Industries
Nr. of Employees
large (251-1000)
Everest Clinical Research
Markham, Ontario, Canada, North America
Services
Statistical design and programming support across all clinical phases, integrated analyses, dataset preparation for submissions, and PK/PD modelling.
CRF/eCRF design, EDC implementation, data cleaning and integration, medical coding, QA sampling, database lock and archival, with user support and training.
Web-based randomization and drug supply management systems with inventory monitoring, automated resupply, reporting and 24/7 support.
Regulatory strategy, gap analysis, agency meeting support, eCTD publishing, submission project management, and ongoing filing maintenance.
Study-level safety plan development, safety database build and integration, case processing, regulatory reporting and integrated safety analyses.
Authoring and e-publishing of regulatory and scientific documents including protocols, CSRs, integrated summaries, and manuscripts using ICH guidance.
Statistical design and programming support across all clinical phases, integrated analyses, dataset preparation for submissions, and PK/PD modelling.
CRF/eCRF design, EDC implementation, data cleaning and integration, medical coding, QA sampling, database lock and archival, with user support and training.
Web-based randomization and drug supply management systems with inventory monitoring, automated resupply, reporting and 24/7 support.
Regulatory strategy, gap analysis, agency meeting support, eCTD publishing, submission project management, and ongoing filing maintenance.
Study-level safety plan development, safety database build and integration, case processing, regulatory reporting and integrated safety analyses.
Authoring and e-publishing of regulatory and scientific documents including protocols, CSRs, integrated summaries, and manuscripts using ICH guidance.
Expertise Areas
- Clinical trial management
- Clinical data management
- Biostatistics and statistical programming
- Pharmacovigilance and drug safety
Key Technologies
- Electronic data capture (EDC)
- Interactive Web Response System (IWRS/IWRS)
- eDiary / ePRO systems
- eCTD publishing and submission gateways