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Small and emerging biopharma like yours face a crucial question – should you outsource your drug safety system, or bring…

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

Every person who wants to participate in clinical research should have the opportunity to do so…

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

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

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

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

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

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

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