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Advance your small molecule from concept to clinic

Move your small molecule forward through discovery, IND and NDA submission with WuXi AppTec's integrated platform. Our comprehensive solutions address bioanalytical, DMPK, and toxicology testing needs while meeting your critical development timelines with expert scientific support at every stage.

Contact our team to learn about our full range of services and capabilities for small molecule development.

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IND Enabling Packages
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In Vitro Studies per Year
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In Vivo Studies per Year

An end-to-end preclinical program 
designed for your small molecule

Our end-to-end small molecule platform combines world-class analytics, experienced toxicologists, and global regulatory knowledge to navigate development hurdles and strengthen your submission package.

Bioanalysis

Put your small molecule candidate on the right track with a bioanalytical strategy designed to establish and execute the right assays for regulatory submission.

DMPK

Leverage a global network of facilities offering a full range of discovery screening, preclinical development, and clinical drug metabolism and pharmacokinetic services.

Toxicology

Our integrated safety assessment services provide multidisciplinary expertise and experience that saves time and cost while yielding the valuable data you need.

Pharmacology

Get validated discovery assays, including in vitro assays and in vivo disease models in cardiovascular, CNS, respiratory, metabolic, and infectious diseases.

CMC

We support your CMC authoring needs, in both the US and China, from preclinical to commercial lifecycle management for drug substance and product. 

Regulatory Affairs

Make global filings convenient, efficient, and cost-effective across US FDA, NMPA, and EMA with our extensive regulatory submission support. 

Your end-to-end preclinical testing partner

With capabilities in safety assessment, DMPK/ADME, bioanalytical, pharmacology, Chemistry, Manufacturing and Controls (CMC) and analytical services all under one roof, WuXi AppTec is a global expert in preclinical development testing and can support the full scope of your development program, from discovery to IND-enabling studies to NDA submission.