VxP Pharma, offers stand-alone drug development services, as well as complete development support for pharmaceutical and biotech projects from discovery, through formulation and clinical trial materials, to niche commercial manufacturing. Most of our locations, including in North America, Europe and Asia, have been US-FDA inspected, and all have a long track record of successful collaborations with Global Pharma clients, Virtual Companies, and everything in between.

VxP offers an extensive range of preclinical services to help you in the drug development process by designing, managing, and documenting your safety tests to meet regulatory requirements for your IND-enabling program.

With decades of experience working with polymorphs, salts, amorphous solid dispersions, and cocrystals, our solid state scientists are among the industry’s best. We can help you identify, understand, and enhance your compound’s properties.

VxP Pharma provides expert formulation development & pharmaceutical contract manufacturing services for virtually any dosage form. We can help bring your molecule to market quickly and cost effectively.

VxP Pharma’s team of experienced scientists can assist you in all stages of your sterile project, from lyophilization cycle development and optimization to commercial manufacturing of lyophilized products.

VxP Pharma offers parenteral development, microbiologic support, and cGMP manufacturing for both liquid and lyophilized products. Our isolator technology provides ISO class 5 processing and containment for both potent and cytotoxic products.

VxP Pharma Services provides product development, scale–up and commercial manufacturing services for virtually every dosage form on the global pharmaceutical market.