VxP Pharma Services is a CDMO offering state of the art contract development and manufacturing services, as well as comprehensive preclinical support, for both small molecule and biologics programs. Our labs are US-based and have been successfully audited by many global regulatory agencies, including the US-FDA. Our contract manufacturing capabilities range from the manufacture of GLP tox supplies, to clinical trial materials, all the way up to and including commercial manufacturing for multiple dosage forms including parenteral and lyophilized products.
VxP Pharma is currently working with most of the world’s largest pharma companies, as well as countless small and virtual companies. Whether you’re wearing many development hats an entrepreneur at a small/virtual company, or a specialist at a large pharma company, chances are good that we have worked on a project similar to yours. Our subject matter experts are among that industry’s best and working together, we can help you navigate your complex development challenges, as well as regulatory hurdles from Discovery through Commercialization. We will truly be your partner in development and beyond.