Preclinical Research Services

Medicilon is a Preclinical Research Outsourcing (CRO) company. With our more than 10 years experience on preclinical research services, we dedicated to provide our clients with customized preclinical services program in drug metabolism, pharmacokinetics, efficacy studies, and toxicology. We provide our clients a high-quality data and rapid turnaround time to support their drug development, preclinical studies and clinical research and to help them to select the most valuable drug candidates into clinical trials stage.

Medicilon's preclinical research services consist in three major parts: pharmacokinetics, disease transplantation models and drug safety evaluation. Our preclinical research services cover all of the aspects including design, in vivo studies, sample analysis, professional data analysis, IACUC review, and the preparation of application materials.

Preclinical Research Services

Quick start experiments and flexible experimental design help you to speed up your decisions and lower your research cost.
Medicilon's Preclinical Research Division services include toxicology, pharmacology and efficacy studies, absorption, distribution, metabolism, and excretion (ADME), drug metabolism and pharmacokinetics (DMPK), as well as bioanalytical solutions for small molecules, biologics, and medicinal herbs.
Drug Metabolism and PharmacokineticsPharmacology Services (Animal Models)Preclinical Drug Safety Evaluation GLP & NON-GLPBioanalysis

Perfect and Complete Preclinical Research Laboratories

Medicilon's labs are certified by Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC) and comply with the GLP standard of US FDA and NMPA. Our preclinical safety evaluations also comply with the Organization for Economic Cooperation and Development in Europe (OECD) GLP requirements.
We maintain a large in-house library of animal disease models to meet the research demands in different therapeutic areas. Medicilon can also assist clients in the preparation of a preclinical safety evaluation package.

Certification

Medicilon is one of the CRO to offer preclinical animal testing service for the global pharmaceutical companies in China. Some of the platform provided by Medicilon such as Drugs Safety Evaluation for Non-Human Primates Services Platform and Isotope Drug Metabolism Professional Services Platform is certified by Shanghai government. In addition, our platform is certified and identified as an important drug discovery platform by Shanghai government.

Medicilon’s Advantages

Extensive pharmaceutical drug discovery and development expertise in small molecules (NCE), biologics, and medicinal herbs for any therapeutic modalitiesFull AAALAC accredited laboratories and facilities200⁺ oncology models and 100⁺ non-tumor disease models for safety and efficacy assessmentA full range of bioanalytical services and global regulatory affairs to enable successful IND submissionIT platforms such as Watson LIMS software and Provantis ensure seamless data collaboration, submission (SEND format), and securityDedicated research scientists with flexible capacity

Service Cases

Medicilon Assists | China's First CD19×CD3×CD28 Trispecific Antibody Obtained FDA Implicit Approval.webp

Medicilon Assists | China's First CD19×CD3×CD28 Trispecific Antibody Obtained FDA Implicit Approval

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Medicilon Assistant| Jimincare's lgE Antibody Drug JYB1904 has been Approved for Clinical Trials.webp

Medicilon Assistant| Jimincare's lgE Antibody Drug JYB1904 has been Approved for Clinical Trials

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Sinovent's New Class 1 Anti-tumor Drug XNW14010 has been Approved for Clinical Trials.webp

Sinovent's New Class 1 Anti-tumor Drug XNW14010 has been Approved for Clinical Trials

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