Services
Our services
Expert support across the drug development lifecycle.
Clinical Pharmacology and Human Pharmacokinetics
Design and oversight of clinical pharmacology studies, CRO placement, PK analysis and reporting from pre-IND through development.
Learn more →Toxicokinetics and Animal PK-PD Studies
Pre-clinical safety, toxicology and GLP studies to enable INDs and support entry into clinical development.
Learn more →Modelling & Simulation
Population PK, PK-PD, exposure-response and dose optimization to guide development and save time and cost.
Learn more →Translational Medicine Studies
Maximize gain from early data—signs and markers that guide decision-making, program design and endpoint selection.
Learn more →Early Development for Start-ups and Mid-size Pharma
Efficient early development function from pre-IND through proof-of-concept for companies without in-house capacity.
Learn more →Regulatory Interactions and Submissions
Regulatory strategy, briefing packages, meeting support and agency alignment with FDA, EMA, MHRA and PMDA.
Learn more →Due Diligence
Scientific and regulatory due diligence for licensing and acquisition—assessment and preparation for investors.
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