Adaptive by Design Trials Good study design includes thoughtful planning and involves bringing subject matter experts, like statisticians, in early. Statisticians can take existing or historic trial data for a particular disease area and create hypothetical scenarios that can inform the shaping of a tighter,
The Statistician’s view of a Clinical Trial The typical flow of clinical trial data begins with the patient and ends with a clinical study report or publication. In between, data passes through a number of steps from collection to verification to analysis. Most stakeholders in
What is Real World Evidence? The relatively new practice of Real World Evidence (RWE) has proven to greatly enhance the quality and effectiveness of clinical studies. According to the FDA, Real world evidence is the clinical evidence regarding the usage and potential benefits or risks
