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Pharmaron is a leading life science contract research organization providing comprehensive drug discovery, development, and manufacturing services to pharmaceutical and biotech companies worldwide.
Pharmaron is a premier Contract Research Organization (CRO) dedicated to accelerating the discovery and development of novel therapeutics. With a global presence and state-of-the-art facilities, we support pharmaceutical, biotechnology, and medical device companies across the entire drug development lifecycle.
Our mission is to deliver high-quality, integrated services with scientific excellence, operational efficiency, and regulatory compliance. From early discovery to clinical development and commercial manufacturing, Pharmaron empowers innovators to bring life-changing medicines to patients faster.
Scientific Experts
Global Locations
From discovery to clinical trials, Pharmaron offers end-to-end solutions tailored to your project needs.
Full-service discovery support including medicinal chemistry, biology, DMPK, and safety assessment to advance your molecule from hit to IND.
End-to-end CMC services for small molecules and biologics, including process development, analytical testing, and GMP manufacturing.
GLP-compliant toxicology studies including general toxicology, safety pharmacology, genetic toxicology, and pathology.
Advanced bioanalytical solutions for small and large molecules, including biomarker analysis and carbon-14 bioanalysis.
Early-phase clinical trials, vaccine development, and human ADME studies using radiolabelled compounds.
IND-enabling services, cell line development, process optimization, and analytical support for biologics and advanced therapies.
Explore our advanced platforms and targeted service offerings.
Hit-to-lead optimization, SAR studies, and synthesis of novel scaffolds including heterocycles and nucleosides.
Custom peptide synthesis, protein engineering, and antibody discovery platforms.
Carbon-14 and tritium labelling for metabolism, PK, and mass balance studies.
Ultra-sensitive detection for microdosing, mass balance, and metabolite profiling.
Cell-based assays, kinase profiling, biophysics, and cellular disease models.
Oncology, CNS, metabolic, inflammation, and ocular disease models.
Hit discovery using billion-compound libraries and advanced screening.
Preclinical and clinical formulation design for optimal bioavailability.
All services adhere to global regulatory standards for quality and compliance.
Rapid turnaround times and flexible project management to meet your milestones.
Access to world-class scientists across diverse therapeutic and technical domains.
Operations across North America, Europe, and Asia with seamless project coordination.
Pharmaron provides integrated services across drug discovery, development, and manufacturing, including medicinal chemistry, biology, DMPK, safety assessment, CMC, bioanalysis, and clinical development.
Yes, all Pharmaron laboratories and manufacturing sites operate under GLP and GMP standards with regular audits and certifications.
Yes, we offer comprehensive radiolabelling services including carbon-14 and tritium synthesis, AMS analysis, and human ADME studies.
Yes, we provide end-to-end support for biologics, including antibody discovery, cell line development, process optimization, and IND-enabling studies.
Ready to discuss your project? Reach out to our team of experts to learn how Pharmaron can support your drug development journey.
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