eMDR e-book: 7 Tips for Transitioning to Electronic Medical Device Reporting
The electronic reporting revolution is here. Is your organization achieving eMDR success?
Beginning August 14, 2015, FDA regulations now require all adverse event reports to be submitted electronically.
Download this e-book to learn best practices for eMDR submissions including lessons learned from the success other regulated companies have already achieved.
Download this e-book to learn more. »