At our US-based, US-FDA inspected facilities, we offer a wide range of services ranging from R&D Scale – including tox supplies, to clinical trial materials to niche commercial manufacturing. We work with multiple dosage forms including sterile injectables (vials and Pre-filled syringes) and lyophilized products for biologics, including live virus, and also for small molecule programs.

In addition to CDMO services, VxP’s preclinical group offers a complete range of in-vivo and in-vitro preclinical safety evaluation studies in support of IND and NDA submissions to the US FDA and other global regulatory authorities.