How does Mission3 OnDemand handle regulatory submissions?
Mission3 OnDemand regulatory submission management application delivers both significant operational efficiency and tremendous time-to-market advantage. By integrating our document management system submissions can be linked to documents while the work on documents are underway. This enables the submission to be ready when all the work is done. Additionally, Mission3 OnDemand allows you to clone submissions to create regional or derivative submissions. You can reuse content and edit only the parts of a submission that need to change resulting in a significant reduction in time, effort, and resources. Back to Top Q: My compounds are in clinical trials, is it too early to implement Mission3 OnDemand? A: The earlier the better. Deploying Mission3 OnDemand just prior to Phase 1 clinical trials allows you to start the product development process in a more organized fashion. It allows you to quickly allocate resources, collaborate between internal and external resources reducing the amount o
