High-quality integrated pharmacometric modeling & simulation services, allowing client organizations to overcome a shortage of resources or expertise. IntiQuan can support your projects in all phases of drug development and help you leveraging your data for informed decision making.
Clinical Pharmacology is the heart of clinical development, probing the drug actions/effects with drug/metabolite(s) concentrations achieved in the system. The early and complete understanding of Clinical Pharmacology aspects renders a successful design of the overall drug development package.
We aspire to be your ideal partner to enable seamless development of your nonclincal and/or clinical programs. We can help in transitioning of your asset to the next decision step by supporting design, study conduct, and data interpretation of a single study or multiple studies.
Our Regulatory Advice begins with laying out a clear strategy and framework to ensure the program meets the requirements of the Regulatory Agencies. We can provide guidance with respect to the FDA expectations and tease out issue(s) of criticality from the FDA perspective.
We can support your project with fit-for-purpose analyses that leverage your data for informed decision making and/or important regulatory interactions
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Comprehensive services in Clinical Pharmacology, Drug Development, ADME/DMPK, and Regulatory Advice & Interactions aimed at increasing the value of your asset
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Our strategic partner esqLABS is a Biosimulation CRO for PBPK-based analyses to support Formulation Development, evaluation of Drug-Drug Interactions, Pediatric and Geriatric Extrapolation Plans, and Organ-impairment Studies.
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We develop and provide powerful and user-friendly computational tools and workflow solutions that support high efficiency & quality, low inter-analyst variability, and 100% reproducibility at any time
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