MasterControl News Archive

On average, around 4,500 drugs and medical devices are pulled from shelves across the United States each year.1 This alarming statistic underscores the importance of controlling and mitigating risk in healthcare-related products. Recent updates to regulatory guidances and standards are encouraging life sciences companies to step up their risk management efforts by infusing risk-based thinking into their entire quality ecosystem.

Read the full article here: Why Risk-Based Thinking Is Essential in Medical Device Development