In today’s fast-paced clinical research landscape, time is money—literally. The ability to streamline processes, reduce time spent on manual tasks, and cut costs is crucial for success. At Clinials, we understand this, and that’s why our platform is designed to create tangible Return on Investment (ROI) for our customers, particularly Contract Research Organizations (CROs) and… Continue reading Maximizing ROI with Clinials: How Our Platform Streamlines Clinical Trial Operations
What are the top key pain points for Sites and CRO’s? Here’s a table from this comprehensive study of site engagement literature conducted by the Tufts University CSDD to identify the primary themes and “pain points” or challenges that sites contend with on a regular basis, including those captured by SCRS. How does Clinials… Continue reading Key Pain Points for CRO’s and Sites
Clinials were the first to use AI to generate a plain language synopsis (PLS) from a protocol Completed in 2022, this innovation was in response to European Union Clinical Trial Regulation 536 EU which mandated that a a summary be “written in a manner that is understandable to laypersons”. And now we have another first.… Continue reading What is a Plain Language Protocol Synopsis (PLPS)
Upcoming Layperson/Plain Language Summary (PLS) Regulations The much-anticipated 2014 European Union Clinical Trial Regulation 536 (EU CTR) requiring the sponsors and academic researchers conducting research trials to draft layperson/plain language summaries (PLS) is set to go into effect in 2023. The regulation will most likely flow to other countries and will be adopted by various… Continue reading Upcoming Layperson/Plain Language Summary (PLS) Regulations
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