White Paper - The Challenge of Regulatory Information Management

Regulatory Information Management (RIM) has been an emerging life sciences industry practice over recent years. At its inception RIM was focused upon adding a degree of intelligence to the management of the global product registration process, by answering questions such as:

  • Which products do we have registered and in which markets?
  • When is the license renewal for product X due?
  • What are the approved product characteristics?
  • Where do I need to submit product changes?
  • Which health authority responses need preparing and when are they due?
  • What actions did I commit to the health authorities?
  • Where do we have authorised products that are not marketed?

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