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 |
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Protocol, CRF Design, Data Management, Statistic analysis and Medical writing |
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Site Selection and Training | ![]() |
Post Marketing Surveillance Programs and Pharmacovigilance | ||||||
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Project and Site Management Services | ![]() |
Pharmacoeconomic Research and Analysis | ||||||
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Clinical Monitoring Services Importation, Storage, Distribution and Destruction through authorized depots |
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Clinical Research and Pharmacology Consulting | ||||||
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Medical Affairs Support and Consulting | ||||||||
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Local Medical Monitoring and Adverse Event Reporting and Management | ![]() |
Tailored Medical Training Programs (All therapeutic areas, New drug and GCP) | ||||||
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Clinical Supply Management: | ||||||||
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Investigator / Site Contract Negotiation and Payment Administration | ||||||||
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