VxP Pharma Services offers state of the art contract development and manufacturing services, as well as comprehensive preclinical support, for both small molecule and biologics programs. We have extensive experience with a wide range of dosage forms, including: Solid Oral, Liquid Oral, Semi-Solid, Transdermal, Solid Dispersions, Sterile, and lyophilized products to name a few. The majority of our facilities are US-based, and most are US-FDA audited. Our contract manufacturing capabilities range from tox supplies, to clinical trial materials, all the way up to and including commercial manufacturing. We offer extremely competitive pricing on generics, and “tail-end” products, as well as full development and CTM manufacturing of complex formulations, in multiple dosage forms, for your IND-enabling studies.
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 an entrepreneur at a small virtual company who wears many development hats, 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 can help you navigate complex development challenges, as well as regulatory hurdles from Discovery through Commercialization. We will truly be your partner in development and beyond.
VxP can deliver the services and the solutions that you need to get your molecule into the clinic, and on the fast track to market.
VxP’s focus includes:
- Preclinical Services
- Preformulation & Solid State Chemistry
- Analytical & Bioanalytical
- Formulation Development
- cGMP Clinical Trial Materials Manufacturing
- Parenteral and Lyophilized Clinical Trial Materials
- Commercial Services
VxP can provide the guidance, the services, and the expertise necessary to accelerate your development program to help get your molecule into the clinic, and to market, in an efficient and cost effective manner.