has the technical and business expertise
necessary to deliver critical solutions
that meet the specific demands of organizations
within the Life Sciences sector.
By pairing our Technologists with compliance
specialists, TechnoVision has effectively
delivered information technology and Business
Process Solutions that enable companies
to effectively manage their clinical trial
information, FDA 21 CFR Part 11 compliance
regulations pertaining to electronic document
submission for New Drug Applications as
well Process Automation Techniques.