Clinical Operation

 

Model: CO

Category: *CRO

Exhibitor: EFFICIENT PHARMA MANAGEMENT CORP.

Booth No: M1117

 

Characteristic

 

EffPha provides integrated services spanning clinical study design, regulatory services, clinical study management & monitoring, data management, and biostatistical analysis. We have extensive experience across Phase I to Phase III clinical studies, with particular expertise in early-phase oncology trials. Our cross-functional team delivers customized solutions that balance budget, timeline, and quality. Leveraging our experts’ global drug development experience and strong international partnerships, EffPha is well-positioned to support multinational clinical trials that meet international standards.

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

 

Other Products

 

• 

  Scientific Evaluation & Support

• 

  Regulatory Service

• 

  Biostatistical Analysis

• 

  Data Management

• 

  Non-Clinical Study Management

 

 

 

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