VxP Pharma offers a full range of contract development and manufacturing services, as well as technical and regulatory support, for the development and production of pharmaceuticals and biologics products. We offer cGMP contract manufacturing of most forms, through all phases of clinical trials, as well as commercial manufacturing dosage.
Our subject matter experts are among the industry’s best, and can provide the expertise required to accelerate your development program, and move your molecule into the clinic, and on into the market in an efficient and cost effective manner.
VxP Pharma Services
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.
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 development and manufacture of sterile solutions, dispersions, suspensions, emulsions, liposomes, and nano-particles for ophthalmic products.