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EPS

EPS, established in 1991, is a leading Japanese CRO with 1,800 employees helping global customers rediscover and appreciate true value in the Asian markets, including Japan, China, South Korea, Hong Kong (China), Singapore and Taiwan (China). EPS remains the clients' first choice in monitoring, data management and biostatistics with dynamic assignment algorithms and in the therapeutic area of Oncology due to its distinguished expertise and achievements through 1,300 protocols of Phase I-IV, post-marketing surveillance and doctor-led studies, incorporating e-Clinical Technology and in combination with related services including pre-clinical testing, Medical Writing, GCP-Auditing, SMO and CSO for a seamless integrated solution.

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Locations

APAC

Overview Accreditations

Therapeutic Areas

Bone / Osteoporosis
Cardiovascular
CNS
Dental and Oral Health
Dermatology
Diabetes
Endocrinology
Gastroenterology
Genetic Diseases
Hematology
Hepatology
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

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 eCOA application, best 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, or by a Clinician. Patients enter their patient data through a provisioned device or their own device after downloading the appropriate app. Clinicians enter patient data through a provisioned device (Android or iOS). eCOA 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.