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 (parenteral) and lyophilized products.  In addition to CDMO services, VxP 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.