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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…

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

Why Having a Well-Prepared eTMF is Important A well-prepared Electronic Trial Master File (eTMF) is critical to the success of…

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…

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

When saddled with legacy medical information systems, Medical Affairs teams are forced to behave like detectives, hunting down information…

The coronavirus pandemic ushered in a new era of public scrutiny for the pharmaceutical industry. The general population was…