Regulatory Information Management (RIM)

Regulatory requirements can feel like barriers on your journey to introducing a new pharmaceutical.

Regulatory Information Management (RIM) impacts development, capture, dissemination, control and management of regulatory-focused content, throughout the product lifecycle.

RIM also involves many departments of a Pharmaceutical company, such as, Drug development, Drug Safety / Pharmacovigilance, Regulatory Affairs / Regulatory Operations, Product Labeling, etc.

USDM Life Sciences is the leading provider to global life sciences companies of comprehensive support services that can help navigate you through the RIM waters with the following:

  • RIM System readiness and Current State assessment  
  • Project Management and Implementation support (partner with RIM vendors)  
  • Validation  
  • Testing  
  • Planning and Strategy 

Contact USDM today for assistance with your RIM needs.

Testimonials

  • Clintrak - Jeffrey D. Coffin
    I have had the great pleasure to work with Bob for 5 years in his position of VP of Quality at Fisher Packaging Services while I acted as Director of Quality services at a sister…
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