Meaning – The Conqueror of Most Maladies

A biomedical professional is certain to have come across some variant of the headlines mentioned in the visual above. Combinations of trending buzzwords in technology and healthcare form half of my...

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Q&A with Dan Szot, Our New VP Sales, Life Sciences and Healthcare

We’d like to introduce you to the newest member of our team, Dan Szot, who has joined us as VP Sales, Life Sciences and Healthcare. Dan brings more than 20 years of sales leadership and field...

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Accelerating Insight - Smart Data Lake Customer Success Stories [Slideshare]

At Gartner's Data & Analytics Summit 2017, Alok Prasad, President of Cambridge Semantics, was joined by Peter Horowitz of PricewaterhouseCoopers for their session entitled “Accelerating Insight:...

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Riding The Competitive Intelligence Automation Wave - Part 1

“If you know the enemy and know yourself, you need not fear the result of a hundred battles. If you know yourself but not the enemy, for every victory gained you will also suffer a defeat. If you...

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[Slideshare] Smart Data Lakes: Revolutionizing Enterprise Analytics

At Strata+Hadoop World 2016, the concept on everyone's mind was the Data Lake. Fortunately, Marty Loughlin, our Vice President of Financial Services, was there to discuss how Smart Data Lakes are...

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2016 Life Sciences Smart Data Discovery & Analytics Forum [Slideshare]

Last month, Cambridge Semantics held its inaugural Life Sciences Smart Data Discovery and Analytics Forum in Boston. At this forum, leaders in Life Sciences and Big Data met to discuss the...

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CDISC and Smart Data Lakes: Extracting Value from Clinical Trial Data

In the pharmaceutical world, clinical trials are essential to any medical research study, such as testing the benefits and risks of a specific medical treatment or drug. But because massive amounts...

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Simplify Clinical Trials Metadata Management with Semantic Technology

The FDA has adopted the CDISC SDTM standard for clinical trial submission. While the standard has the potential to simplify the reporting processes, adoption poses challenges to and raises questions...

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With CDISC Adoption by FDA, Managing Clinical Trial Metadata with Semantic Technology Has Emerged Front and Center!

As FDA outlines, “the submission of standardized study data enhances a reviewer’s ability to more fully understand and characterize the efficacy and safety of a medical product,” and adopted CDISC...

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