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Reading Time: 3 minutes Many people may believe that if an integration works, it was created the right way. The reality is that an integration working correctly is not necessarily an indication that it was built using the best available methods and, moreover, that it will continue to work correctly five years down the road. Technologies change, products get upgraded, colleagues come and go, data models are modified and of course software has an irritating way of getting “brittle.”

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Reading Time: 2 minutes Isn’t it great when you get really good, helpful customer service?

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Reading Time: 2 minutes It’s no secret that clinical trial complexity and drug development costs are at an all-time high. With more than 30 percent of trial budgets allocated to site monitoring costs—and more than half of that being spent on source document verification (SDV) activities¹—the idea of implementing a risk-based monitoring (RBM) program to rid ourselves of the traditional 100-percent-SDV approach has the life sciences industry buzzing.

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Reading Time: < 1 minutes We recently sat down with Robert Musterer, president of ER Squared, an eClinical consulting company partnering with Zifo Technologies. Robert presented at the Medidata Symposium on “Overcoming Inertia for Improved Clinical Trial Designs,” a topic he covered in this recent Geeks Talk Clinical blog post.

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