Developing a new medical device can take anywhere from 18 months to 5 years. This is further complicated when registering a device in multiple countries and regions. MasterControl Regulatory Excellence can help you collect, manage and submit all the artifacts you need, regardless of which regulatory body you’re dealing with.
Regulatory Excellence makes regulatory information management, registrations and submissions simpler processes. The solution lets you automate your dossier management processes and the collection, review and approval of all related documents. You can track different requirements for every geographic location and our preconfigured templates help you launch a project faster.
