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A cautionary tale from pharma offers lessons to device manufacturers about the dangers of a quality system that isn’t digital.
May 27, 2021
By: Dale Thompson
Contract manufacturing and contract development manufacturing organizations (CMOs and CDMOs) remain in the spotlight for helping to make it possible to produce COVID-19 vaccines, which are needed around the world. As of mid-May, about 9.7 percent of the world’s population has been vaccinated against COVID-19, which equates to 1.48 billion doses.1 With all eyes on the contract manufacturing industry, increased scrutiny brings the issue of maintaining quality to the forefront. It’s a significant challenge to manufacture a product at the quick pace demanded by customers while maintaining impeccable quality. Managing multiple, changing product lines increases complexity and the difficulty of maintaining speed as well as quality. With a modern manufacturing solution, CMOs and CDMOs can prioritize both. Costs of Compromising Quality Emergent BioSolutions was rushing to manufacture vaccines for Johnson & Johnson and AstraZeneca at their plant based in Maryland, and a production error led the CDMO to scrap the materials for up to 15 million Johnson & Johnson vaccine doses.2 In April 2020, the U.S. Food and Drug Administration (FDA) issued a Form 483, which noted several quality control issues at Emergent’s manufacturing site that led to the cross contamination of materials including a lack of written procedures and inadequate operator training.3 Now the FDA is questioning whether or not the equivalent of 70 million doses from the same plant can be distributed, and executives from Emergent BioSolutions will testify before the House Select Subcommittee on the Coronavirus.4,5 No CMO or CDMO wants to find themselves in a similar position. In the race to keep up with demand, losing sight of quality can jeopardize compliance. More importantly, it can result in longer wait times for people who need life-saving products. Improve Quality with Digitization The likelihood of encountering problems like those experienced by Emergent BioSolutions (i.e., lack of written procedures and inadequate training) can be greatly reduced with a fully integrated, digital platform where standard operating procedures (SOPs), training documents, and production records can be managed from a central location. By operating from a connected system, it is possible to embed quality into every stage of production. The National Institute of Standards and Technology reported that investing in advanced technology delivers benefits such as:
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