VxP Biologics offers the convenience of a central “One Stop Shop” CRO, combined with the advantages of working with a specialist “Niche CRO.” We’re able to deliver this unique capability because each facility is independently owned and operated, and specializes in only one area of development.
We can help you navigate complex development problems, as well as regulatory hurdles. When you work with VxP Biologics, you will collaborate directly with dedicated experts in each area of development, and not simply a “generalist” who happens to be assigned to your project.
Our service-specific focus and dedication to quality has insured that much of our business comes from returning customers. We fully understand that our clients are looking for:
- Ready Access to our Subject Matter Experts
- Dedication to Meeting Time Lines
- Competitive Pricing
Although most operations are located in the United States, some facilities are located in Europe and Asia. The majority of these sites have been US-FDA audited, and all have a long track record of successful collaborations with global biopharma clients, virtual companies, and everything in between. Whether you’re an entrepreneur at a small virtual company who wears many development hats, or a specialist at a large biopharma company, VxP Biologics 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 Services include:
- Analytical & Bioanalytical
- Formulation Development
- cGMP Clinical Trial Materials Manufacturing
- Parenteral and Lyophilized Clinical Trial Materials
- Biologics Development and cGMP Cell Banking
VxP can provide the guidance, the services, and the expertise necessary to accelerate your development program to help get your biologic into the clinic, and to market, in an efficient and cost effective manner.