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Learn how you can move to the next generation Regulatory Content Management platform, including the critical task of managing correspondence with regulatory agencies.  USDM Life Sciences can provide project management, requirements development, validation and more.  Generis’ CARA can be used for Regulatory Affairs, Submission Management and Correspondence Management with one single user interface.  Generis will demo key features of CARA for Regulatory Correspondence Management.

The discussion will include:
  • Overview of how CARA can be used for regulatory correspondence management and tie into existing submission systems
  • How to avoid data migrations and allow users to access and manage information through a single user interface
  • How USDM Life Sciences can help you implement the new platform
  • Live Q & A session
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