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EPS

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EPS

EPS launched its business in 1991 and has grown to be a Top Tier CRO comprehensively supporting clinical trials and post marketing surveillance. The company proposes new models to satisfy customers’ needs by leveraging its data science expertise and digital technology, cultivated through its extensive track record. These service offerings are anchored in its Trial GATE concept, which acts as the gateway for clients for access to all clinical trial functions.

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Locations

  • APAC
  • North America
Overview Accreditations / Enablement

Therapeutic Areas

  • Bone / Osteoporosis
  • Cardiovascular
  • CNS
  • Dental and Oral Health
  • Dermatology
  • Diabetes
  • Endocrinology
  • Gastroenterology
  • Genetic Diseases
  • Hematology
  • Immunology
  • Infectious Diseases
  • Inflammation
  • Internal Diseases
  • Metabolic Diseases
  • Musculoskeletal
  • Nephrology
  • Neurology
  • Nutrition and Health
  • Obstetrics / Gynecology
  • Oncology
  • Ophthalmology
  • Orthopedics
  • Otolaryngology/ENT (Ear/Nose/Throat)
  • Pediatrics / Neonatology
  • Pharmacology / Toxicology
  • Podiatry
  • Psychiatry
  • Pulmonary
  • Respiratory
  • Rheumatology
  • Sensory Organs
  • Sleep
  • Thrombosis
  • Urology
  • Vaccines

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 accreditation.
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+ Domains. Coder+ Accreditation is dependent on the successful completion of the Rave accreditation.
Partners are trained on the functionality of the eCOA applications, best operational and project management practices, process optimization and the scope of eCOA services. This Accreditation teaches Partners to process patient data that has been entered by the patient themselves, supporting participants or by a Clinician. Patients enter their patient data through a provisioned device or their own device (Android or iOS) after downloading the appropriate app, or through the myMedidata Website. Clinicians enter patient data through a provisioned device. eCOA Accreditation is dependent on the successful completion of the Rave 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 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 Accreditation.