Clinical Operation

 

Category: *CRO

Exhibitor: EFFICIENT PHARMA MANAGEMENT CORP.

Booth No: M820

 

Characteristic

 

EffPha expertise in early phase clinical research, especially Phase I and Phase II studies. With our multi-disciplinary experts that specializes in different areas of drug development, we are able to provide the most demanding clinical service and complete projects on time, on budget with the best quality. With our know-how of our experienced experts and global partners, we are capable of providing multinational scale studies that meet global standards.

We deliver the following services:
- Clinical Study Planning
． Site and PI Selection
． IRB Document Preparation and Submission
． Clinical Site Initiation
- Clinical Study Management and Monitoring (Phase I-IV)
． PI Meeting
． Study Planning and Preparation
． Study Execution and Monitoring
． Health Authorities’ Inspection
． Site Audit
- Medical Monitoring

 

Other Products

 

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  Data Management

• 

  Regulatory Service

• 

  Statistical Analysis

• 

  Regulatory Service and Clinical Operation for Drug Development

• 

  Non-Clinical Study Management

• 

  Scientific Evaluation & Support

 

 

 

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