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Look at paperwork and regulations

Nothing evolves within a vacuum. While today we can transmit reports, research, and more at the click of…

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The management of data within organizations has far-reaching effects, as interconnected data provides valuable insights that can yield positive…

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Most regulatory information management (RIM) systems were designed to capture essential regulatory data elements, e.g., drug substance and drug…

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What is Regulatory Information Management (RIM)?

Regulatory Information Management (RIM) refers to an organization or team’s ability to manage…

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doctor discussing test results

Identification of Medical Products (IDMP) has been harmonizing data globally across the drug development lifecycle since 2003. At its…

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Managing the submission of medicinal products, medical devices, and biologics to regulatory agencies is growing more complicated all the…

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When selecting an IDMP solution, remember decisions made today will impact the organization for years to come After a decade…

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Regulatory teams serve as the common thread of pharmaceutical research and development, connecting each domain on a drug’s journey to approval. Theirs…

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As the pharmaceutical industry adapts to a new world with a new set of challenges, it is critical to keep…

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BREXIT, the withdrawal of the United Kingdom (UK) from the European Union (EU) and the European Atomic Energy Community…

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