Navitas Life Sciences

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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