Scope of Services
 
 

International Phase I-IV Trials

 

Local Phase IIIb-IV Trials

Complete Clinical Trial Regulatory Services
MOH, IRB Submissions and Essential Documents Gathering
Protocol, CRF Design, Data Management,
Statistic analysis and Medical writing
Site Selection and Training Post Marketing Surveillance Programs and Pharmacovigilance
Project and Site Management Services Pharmacoeconomic Research and Analysis
Clinical Monitoring Services
Importation, Storage, Distribution and Destruction through authorized depots

Clinical Research and Pharmacology Consulting
Medical Affairs Support and Consulting
Local Medical Monitoring and Adverse Event Reporting and Management Tailored Medical Training Programs (All therapeutic areas, New drug and GCP)
Clinical Supply Management:    
Investigator / Site Contract Negotiation and Payment Administration    

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