We Provide Speedy and High Quality Services for New Drug Development

EPS supports all services-related data management, statistical analysis, monitoring, design protocols, regulatory application and post-marketing surveillance in clinical study.We are also utilizing benefits of EPS group to support Asian and Global-study with high quality standard by providing clinical development solutions in a timely manner.

Support for Protocol
Drug Allocation
Pharmacovigilance GCP Audit(QA)
Monitoring/Quality Control(QC)
Patient Registration
Data Management
Statistical Analysis
Clinical Study Report
Support for NDA Application Form
Pharmacovigilance
Patient Registration
Data Management
Statistical Analysis
Clinical Study Report

Supported-Studie

  • Clinical Study
  • Other Clinical Studies
  • Post-Marketing Surveillance
  • Investigator-Initiated Study
  • Extensive Epidemiology Surveillance
  • Clinical Investigation

Supported-Areas

Global Clinical Development Services
We provide Asian and Global study with high quality standard through working with leading global CROs world wide and EPS networks in Asian countries.
Data Center Services
In extensive post-marketing surveillance, we provide client-specific data management services with EPS know-how and human resources.
Offshore Data Management Services
Data management is operated offshore at our subsidiary company in China at low-cost operations with high quality and guarantee the same speed as in Japan.

  1. Full-services in clinical study covered from non-clinical study to post-marketing surveillance.
  2. Support mega-study with enriched experiences in oncology and circulatory organs.
  3. Having specialists with expert knowledge and standardized procedures, we guarantee high quality standard services.
  4. Through EPS overseas network, we support Asian and global study.
  5. With accumulated know-how based on experiences we are able to develop clinical study plan.

[ Contact ] Sales Department TEL +81-3-5804-7577 / FAX +81-3-5684-7872

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