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There’s no doubt that the pharmaceutical industry is well into its ‘age of automation’. A…

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Managing your Trial Master File (TMF) is a necessary, and often tedious task for most clinical stakeholders—but it doesn’t have…

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

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Advances in clinical trial design and technology are significant contributors to medical progress. However, they also hamper clinical operations and…

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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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Data is the lifeblood of businesses today. Data informs strategy and measures success across all industries. While some companies…

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Change is the lone constant you can depend on. When it comes to scientific discovery, most of that change…

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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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A well-prepared Trial Master File (TMF) is critical to the success of any clinical trial. Because the TMF tells the…

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Your team’s workload grows by the day. The volume of Safety cases you’re managing increases significantly every year. All the same, the internal pressure to…

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