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.
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.
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.
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.