New Drug Development
Services

EPS supports all services-related data management, statistical analysis, monitoring, design protocols, regulatory application and post-marketing surveillance in clinical study.

Support clinical development for below clinical studies and surveillances.

  • Clinical Study for Prescription Drugs
  • Clinical Study for OTC Drugs
  • Post-Marketing Surveillance
  • Post-Marketing Clinical Study
  • Investigator-Initiated Study
  • Extensive Epidemiology Surveillance

Detailed service contents

Medical Device Development
Services

EPS supports medical device regulatory, clinical study and post-marketing surveillance widely by knowledgeable experienced staff.

Support for general medical device, controlled medical device and high-controlled medical device for below services.

  • Regulatory Application
  • Clinical Study
  • Post-Marketing Surveillance

Detailed service contents

Generic Drug Development
Services

Full-services ranged from study-design to medical writing including measurement of blood concentration levels are available.

Support for Clinical Development and Planning, Consulting and NDA approval.

  • Bioequivalence Study
  • Safety Study

Detailed service contents

Education and Training Services

Based on experienced know-how in CRO, we provide effective uniform education and training services via e-learning and practical classroom lectures by clinical development specialist.

  • Introduction of Clinical Study
  • CRA-Training / CRC-Training /
    MR-Training
  • Classroom Learning
  • Execution of e-Learning Content

Detailed service contents

Enhanced Solutions
The Work Contents

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

[ Last Update ]

Page Top