해외사업부
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Non-Clinical Safty Assessment / DMPK & Bioanalysis
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Non-Clinical Safety Assessment
- General Toxicology
- Safety Pharmacology
- Developmental and Reproductive Toxicology
- Juvenile Animal Study (JAS)
- Genetic Toxicology
- Carcinogenicity Studies
- Ophthalmology Studies
- Inhalation Studies
- Drug Abuse & Substance Dependence
- Immunogenicity and Immunotoxicity
- Special Toxicities
- Clinical Pathology
- Toxicokinetics
- Assessment of radiopharmaceuticals
- Assessment of biohazardous drugs
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DMPK and Bioanalysis
- Test Article Formulation & Analysis
- Method Development and GLP Bio-analysis Method Valideation
- Drug-Drug Interactinons (DDI)
- In Vitro ADME and In Vivo PK Study
- Biomarker Identification
- Element Residues
- Immunology
- Molecular Biology
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Parmacology & Pharmacodynamics
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1) In Vitro Services
- Immune cell typing
- Flow cytometry
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- ELISPOT
- Cytokine release
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2) In Vivo Models:
- Tumors
- Hematological Diseases
- Cardiovascular Diseases
- Neuropsychiatric Diseases
- Respiratory Diseases
- Metabolic Diseases
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- Urologic Diseases
- Immunity Related Diseases
- Digestive Diseases
- Infectious Diseases
- Others
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Certificates & Qualification
NMPA GLP Compliance 2005 / 2010 / 2013 / 2014 / 2017 / 2020 US FDA GLP Compliance 2009 / 2013 / 2016 / 2019 OECD GLP Compliance 2015 / 2017 / 2021 Korean MFDS GLP Compliance 2016 / 2022 Japan PMDA GLP Compliance 2021 AAALAC accreditation 2008 / 2011 / 2014 / 2017 / 2020 CNAS / ILAC-MRA certification 2018 / 2019 / 2020 / 2022