In life sciences companies, core quality
processes such as CAPA deviations and complaints need to be fully
defined and carefully documented in order to comply with FDA
requirements. The real value, however, in automating these processes
comes from connecting them together in an integrated, closed-loop
system.
In this one hour, on-line session we’ll talk through the critical
design features of an integrated quality management system. The session
will include a demonstration of an integrated solution built on
SharePoint and NextDocs technology.
View recorded Webinar