Pharma R&D Today
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The Importance of the Safety Management Plan for Clinical Trials
Posted on June 30th, 2017 by J.-P. Clement MD in Pharmacovigilance
In a world where many operational and strategic clinical trial activities are outsourced to Contract Research Organizations (CROs), the design and content of the Safety Management Plan (SMP) will greatly influence the execution of clinical trial drug safety activities. (more…)
Human Factors are a Risk in Randomized Control Trials
Posted on October 7th, 2016 by Dr Andrew A. Parsons in Pharma R&D
The World Drug Safety Congress took place this month in Munich, and I was very happy to contribute to a panel discussion regarding human factors in drug safety. (more…)
