Cross-functional R&D teams spanning the full drug lifecycle, with multinational and CRO experience.
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Preclinical
Pharmacology, toxicology and PK/PD studies
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Clinical Development
Phase I–IV trial design, execution and data management
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Regulatory
CDE/NMPA submissions and regulatory interactions
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Pharmacovigilance
Post-marketing safety surveillance and signal assessment
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Biostatistics
Trial design, sample sizing and statistical analysis
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Quality
GLP/GCP/GMP compliance across the pipeline