| Scope of Services |
International Phase I-IV Trials |
Local Phase IIIb-IV Trials |
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| Complete Clinical Trial Regulatory Services MOH, IRB Submissions and Essential Documents Gathering |
Protocol, CRF Design, Data Management, Statistic analysis and Medical writing |
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| 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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