4 Ways to Increase Efficiency in Regulatory Process through Document Transformation
Are you seeking to optimize your existing regulatory processes ?
Watch our webinar where we outlined 4 improvement areas:
• Automate the creation of submission ready documents. Comply with all regulatory health authorities’ requirements including PMDA
• Improve your correspondence tracking processes through automated standardization and routing
• Maximize productivity and reduce the risks associated with the creation of repetitive forms
• Lower total costs by optimizing infrastructure and licencing fees.
Join the Alliance of Experts (Generis, Lorenz, PhlexGlobal, DocShifter and QDossier) to understand the optimal RIM solution – intelligently integrated systems.
Intelligent Integration to RIM and Beyond
WEBINAR – 8AM PST / 11AM EST / 4PM UK / 5PM CET
10 July 2019