Every person who wants to participate in clinical research should have the opportunity to do so…
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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…
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Identification of Medical Products (IDMP) has been harmonizing data globally across the drug development lifecycle since 2003.
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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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Get the Guide: When and How to Choose Your First Safety System 
