RIM

Are you ready? Preparing for the new EU MDR implementations

New regulations are in effect, with transition periods ending in 2020 and 2022 Medical and in vitro diagnostic device manufacturers in the EU are likely aware of big changes in…

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RIM as a load-bearing wall for regulatory compliance

“RIM provides an integrated view of regulatory information.” “Affiliates and regions should play a key role in the system.” “RIM is the foundation of the future IDMP implementation.” The quotes…

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How RIM evolved into today’s integrated, data-driven vision

The industry is currently in a period of unprecedented transformation, driven by ongoing shifts in the regulatory sphere from document-driven to data-driven information management. This transition is certain to continue…

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