About WuXi AppTec DMPK
As a global DMPK service provider, we are committed to delivering all clients with high-quality data, precise R&D strategies, and excellent services to meet the unique needs of clients and become the preferred partner for DMPK studies.
WuXi AppTec DMPK Briefly
WuXi AppTec DMPK leverages over 18 years of experience and a track record of over 1,700 successful IND filings. Operating in the United States (New Jersey) and China (Shanghai, Suzhou, Nanjing, and Nantong), it specializes in pharmacokinetics studies. When you partner with WuXi AppTec for drug discovery and development services, you gain access to an integrated worldwide network of facilities that offer a full range of discovery screening, preclinical development, and clinical drug metabolism and pharmacokinetics (DMPK) platforms and services. These include in vitro absorption, distribution, metabolism, excretion (ADME) studies, in vivo pharmacokinetic studies, metabolite profiling and identification studies, radiolabeled compound synthesis, radiolabeled in vivo ADME studies, and Non-GLP bioanalysis.
18+
Years of experience
1,000+
Employees
1,600+
Global clients
1,700+
Successful IND filings supported
200+
Assay types
300k+
In vitro studies each year
20k+
In vivo studies each year
180k+
Samples analyzed per week
About WuXi AppTec
WuXi AppTec is a trusted partner and contributor to the pharmaceutical and life sciences industries, providing R&D and manufacturing services that help advance healthcare innovation. With operations across Asia, Europe, and North America, we offer integrated, end-to-end services through our unique CRDMO (Contract Research, Development, and Manufacturing Organization) platform. We are privileged to work alongside nearly 6,000 partners across 30+ countries, supporting their efforts to bring breakthrough treatments to patients. Guided by our vision that every drug can be made and every disease can be treated, we are committed to advancing breakthroughs for patients—one collaboration at a time.
Why Choose WuXi AppTec DMPK ?
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Fast and Reliable Data Delivery
No lead time for in vitro and in vivo assays
Fast turnaround time
Meet IND and NDA requirements of FDA, NMPA, and EMA
Successfully pass over 15 years of audits
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High-Throughput Automation Platforms
Fully automated in vitro ADME workstation
Fully automated bioanalysis sample pretreatment system
Automatic blood sampling and plasma separation system
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Experienced and Professional Teams
Dedicated study director provides specialized project management
Professional teams dedicated to experimental design, implementation, and report delivery
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High Standard Instruments and Facilities
AAALAC-accredited and intelligent animal facilities
High-precision bioanalytical and identification instruments
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Integrated Service
Screening to IND filing, In vitro and in vivo
Routine small molecules and new modalities
High-efficiency cross-department cooperation within the company
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