by Kiera Blessing | Apr 18, 2022 | Blogs, Regulatory - Blogs, Uncategorized
Managing the submission of medicinal products, medical devices, and biologics to regulatory agencies is growing more complicated all the time. To streamline the processes that go into creating and tracking these submissions, life science organizations are increasingly...
by Kiera Blessing | Mar 30, 2022 | Blogs, MedComm - Blogs
Data is the lifeblood of businesses today. Data informs strategy and measures success across all industries. While some companies now understand its potential, most are still determining how best to leverage their internal data. Medical Information (MI) teams hold...
by Kiera Blessing | Mar 20, 2022 | Blogs, Clinical - Blogs, Uncategorized
Change is the lone constant you can depend on. When it comes to scientific discovery, most of that change – whether it be in smart phones or space travel – has led to greater achievements and efficiencies. Among Clinical trials, however, efficiency continues to be a...
by Kiera Blessing | Mar 7, 2022 | Blogs, Regulatory - Blogs, Uncategorized
When selecting an IDMP solution, remember decisions made today will impact the organization for years to come After a decade of preparation, the new Identification of Medicinal Products (IDMP) standard is poised to go into effect in a few short months. The impending...
by Kiera Blessing | Feb 28, 2022 | Blogs, Clinical - Blogs
A well-prepared Trial Master File (TMF) is critical to the success of any clinical trial. Because the TMF tells the whole story of a study – including every data point collected and decision made – managing it throughout the course of the trial is challenging. The...
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