VxP Pharma, Inc.   

Preclinical

VxP Pharma Preclinical offers a complete range of in-vivo and in-vitro preclinical safety evaluation studies.  We have a long history of providing flexible solutions, accelerated timelines and supporting both cGLP and non-cGLP laboratory services that meet or exceed global regulatory standards/guidelines. We have conducted multiple IND and NDA enabling studies for submission to the US FDA and other global regulatory authorities, and with this experience, we can offer invaluable guidance as you move your project forward.