Blogs

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 have…

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

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…

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

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…