Toxikon is an international CRO with ISO, GMP and GLP accreditations, with over 35 years of experience. We contract and partner with pharma, biotech and medical device industries to deliver exceptional product development services from concept (with animal disease models) to final product (lot release testing).
We provide in vivo capabilities ranging from mice to non-human primates to support your IND/NDA submission. Including analytical services for stability, impurity profiling and bioanalytical PK/TK support.
- Animal disease/efficacy models – Proof of Concept studies in support of ocular drug development (Dry Eyes, Uveitis, Glaucoma, PVR and NV/AMD) and cancer therapies.
- GLP Preclinical toxicology and safety testing (ICH, OECD and ISO10993)
- GMP Stability testing, extractables & leachables and impurity profiling and Tox assessments
- Medical Device chemical charaterization studies and safety assessment
- GMP Lot release testing (import EU/US)