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Phase I-IV full service clinical development |
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Generic drug development |
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Quality Assurance support and audits |
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Regulatory Affairs and Independent Ethics Committee submissions |
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In-depth customized feasibility assessments |
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Investigator identification and unique site management solutions |
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Data Management |
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Biostatistics |
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Randomization, labeling, and packaging, drug storage and customs clearance |
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Pharmacokinetic and pharmacodynamic services |
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Medical writing |
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Pharmacoeconomic studies |
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Training and consultation |
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Regulatory consultation: USA, Europe, Asia, India, and South Africa |