Considering switching from a paper trial master file to an electronic one? There’s no better time than now. According to…
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The Future of Drug Safety Intelligence The future of safety intelligence is closer…
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As part of our commitment to providing the most robust out-of-the-box (OOTB) offering to our safety customers, we recently…
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Small and emerging biopharma like yours face a crucial question – should you outsource your drug safety system, or bring…
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Regulatory Information Management (RIM) refers to an organization or team’s ability to manage…
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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. At its…
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