Full-service CRO
From first study
to approval, in one place.
FDA Full
Package Service
From GLP non-clinical studies to consulting, SEND datasets and submission — we prepare your US FDA IND and NDA together.
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Research Centers
Four teams carry your program
from non-clinical to clinical.
- 1Safety Evaluation CenterGLP toxicology, safety pharmacology, chemical hazard testsMore →
- 2Efficacy Evaluation CenterEfficacy studies in disease animal modelsMore →
- 3BioAnalysis CenterBioanalysis, PK and biomarkersMore →
- 4Clinical Trial BusinessClinical trial operation, monitoring and data managementMore →
Planning a study?
Tell us about your test article, study type and timeline. The responsible team will contact you.
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