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This on demand webcast has been created by Sandra Vignes Subject Matter Expert- Regulatory at ArisGlobal. This on demand webinar will explore how Regulatory Information Management Systems and Services enable life sciences companies to respond nimbly to IDMP and other changing requirements, while ensuring compliance at the same time. Your Regulatory Affairs function will gain insights on:

How Regulatory affairs can handle the increasing workload in terms of registrations, tracking etc

What the upcoming IDMP regulations mean for Regulatory Affairs and how can this function tackle the challenges that will come along with IDMP

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