Before a drug can proceed to the clinical trial stage, its developer must first pinpoint its likelihood of harming people by performing in vitro and in vivo toxicological studies. These studies involve a number of technical complexities, of which the following three are particularly challenging: 1. In vitro toxicology studies provide only limited insight [...]
Manufacturing competencies aren't the only reasons to partner with a contract manufacturing organization (CMO). Throughout every stage of your pharma development process, analytics can help increase efficiency, raise margins, and keep you ahead of your competition in all seven of the following ways: 1. Validation programs characterize useful compounds, streamlining the selection of stable [...]
Rapid virus evolution challenges the medical industry with new strains every year. The Vero cell platform meets these challenges with a streamlined system for the rapid development of novel vaccines. The platform has proven effective at developing vaccines for SARS, avian influenza and other evolving threats, for the following five reasons: 1. Rigorously validated [...]
