Bespoke scientific expertise to expedite your gene therapy program
Gene therapies
Unique in vivo models, complex methods and routes of administration, to streamline your development
Therapeutic area expertise for indications including: neurology, cardiovascular disease, ophthalmology, immunology and more
Custom assay support for preclinical, biomarker-driven clinical trial testing and commercialization of your potential companion diagnostic
Robust global laboratory experience supporting of 7 FDA-approved gene replacement therapies
Whether you’re developing a viral vector-based therapy, such as an adeno-associated virus or lentivirus product, or applying gene editing technologies such as CRISPR/cas9, we’re here to offer you the type of support you need—when you need it—so you can reach your development goals on time and within budget.
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