Everest Clinical Research

Everest Clinical Research

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to some of the best-known pharmaceutical, biotechnology, and medical device companies in the world. Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO across all other clinical development service areas – clinical operations, IRT/IWRS and ePRO/eDiary technologies, pharmacovigilance, DSMB/DMC, pharmacokinetics/ pharmacodynamics, medical writing, regulatory submissions. With headquarters located in Toronto, Ontario, Canada, our second office in Little Falls, New Jersey, and our third office in Shanghai, China, we serve our clients with high quality, responsiveness, and high caliber personnel. Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. We are proud that 95% of our new business and growth is driven by repeat clients and client referrals, a testament to the great work we do. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success. Quality is our backbone, customer-focus is our tradition, flexibility is our strength.

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Locations

  • APAC
  • North America

Therapeutic Areas

  • Cardiovascular
  • CNS
  • Dermatology
  • Diabetes
  • Endocrinology
  • Gastroenterology
  • Genetic Diseases
  • Hematology
  • Hepatology
  • Immunology
  • Infectious Diseases
  • Medical Device
  • Nephrology
  • Neurology
  • Obstetrics / Gynecology
  • Oncology
  • Ophthalmology
  • Pediatrics / Neonatology
  • Psychiatry
  • Pulmonary
  • Rare Disease
  • Respiratory
  • Rheumatology
  • Sleep
  • Surgery
  • Thrombosis
  • Urology
  • Vaccines
  • Virology

Accreditations

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.