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Everest Clinical Research

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Everest Clinical Research

Everest is a full-service global CRO, built on a long-standing foundation of biometrics excellence.

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Locations

  • APAC
  • Australia
  • Europe
  • North America
  • South America
Overview Accreditations / Enablement

Therapeutic Areas

  • Cardiovascular
  • CNS
  • Dermatology
  • Devices and Diagnostics
  • Diabetes
  • Endocrinology
  • Gastroenterology
  • Genetic Diseases
  • Hematology
  • Hepatology
  • Immunology
  • Infectious Diseases
  • Metabolic Diseases
  • Nephrology
  • Neurology
  • Oncology
  • Ophthalmology
  • Pain / Anesthesia
  • Psychiatry
  • Pulmonary
  • Rare Disease
  • Respiratory
  • Rheumatology
  • Vaccines

Everest is a quality and data-driven Contract Research Organization (CRO) delivering comprehensive clinical trial support to pharmaceutical, biotech and medical device companies worldwide. Founded in 2004, Everest has grown from a small biometrics consultancy into a leading full-service CRO with more than 700 employees and over 130 active clients worldwide. Our continued success is driven by high-quality deliverables, exceptional client service, and a culture of flexibility and innovation.

Today, we are proud to provide full-service CRO support, including regulatory strategy, clinical operations, data management, biostatistics and statistical programming, IRT/RTSM, eCOA technology, pharmacovigilance, and medical writing services. While our capabilities and reach have expanded, our commitment to excellence remains. We continue to combine quality-focused infrastructure, high-touch customer service, and motivated teams with extensive therapeutic area expertise to deliver start-to-finish trial services with speed and quality at every step.

Accreditations / Enablement

Partners are trained on the functionality of the Coder application, process optimization, and scope of Coder services. This Accreditation teaches Partners to integrate the medical coding solution with EDC studies and administer Coder segments. Coder Accreditation is dependent on the successful completion of the Rave EDC accreditation.
Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.
Partners are trained on the functionality of the RTSM Application, process optimization, best practices using RTSM, and scope of RTSM services. This Accreditation teaches Partners to conduct randomization and clinical trial supply management services (RTSM). RTSM Accreditation is dependent on the successful completion of the Rave EDC Accreditation.
Partners are trained on the functionality of the targeted source document verification (TSDV) application, process optimization, and scope of TSDV services. This Accreditation teaches Partners to implement TSDV in line with regulatory compliance and data quality strategies. TSDV Accreditation is dependent on the successful completion of the Rave EDC Accreditation.