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Employing a data-driven quality model helps you apply quality processes more holistically throughout the organization.
April 9, 2021
By: David Jensen, Staff Writer, MasterControl
On several occasions, Acting Commissioner of the U.S. Food and Drug Administration (FDA) Janet Woodcock has called attention to the importance of quality in product manufacturing. Given the high rate of drug shortages, she stresses that quality goes beyond simply meeting the FDA’s current good manufacturing practice (CGMP) requirements. Quality in manufacturing is the ability to reliably produce products in sufficient quantities to ensure that supply meets demand. “Analysis of recent drug shortages indicates the need for rewarding more investment in quality. A team of FDA economists examined a sample of 163 drugs that first went into shortage between calendar years 2013 and 2017. They found that of the 163 drugs in shortage, 62 percent went into shortage after supply disruptions that were associated with manufacturing or product quality problems,” said Woodcock. Data’s Pivotal Role in Quality Life sciences companies have long generated vast amounts of data as a byproduct of their processes for developing and manufacturing products. Quality is one area of the business that is particularly dependent on data. Comparatively, quality gathers and uses more data than other business units in an organization. As long as companies follow the regulatory guidelines for data management and have the required documentation in place, they can achieve regulatory compliance. However, quality processes that involve compiling and storing data on paper documents require more time and effort than is necessary. In fact, it fosters more of a reactive rather than proactive approach to quality. Quality managers often need to spend more time double checking documents and following up with stakeholders to ensure records are complete and accurate. The challenges associated with this approach include:
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