Improving FDA metrics and ‘quality culture’

CPhI Worldwide experts propose new FDA quality metrics system and recommend critical formulation attributes

DDNews Staff
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AMSTERDAM, The Netherlands—This fall, CPhI Worldwide, organized by UBM EMEA, announced the findings of part one of the “2016 CPhI Annual Report” on potential new approaches to improve quality and manufacturing process in pharmaceutical production ahead of CPhI Worldwide 2016 in Barcelona, Spain. As CPhI noted, five world-renowned experts—Ajaz Hussain, Girish Malhotra, Brian Carlin, Pabir Basu and Thomas Friedli—propose improved methods to how we evaluate and consider quality in the pharmaceutical industry, making a number of key recommendations.
According to CPhI, the overall findings reveal there are a number of improvements industry and the regulators can and should make to shift the industry from just meeting standards towards instilling continuous improvement and quality cultures across the board, which the panel predicted will vastly improve overall quality and reduce manufacturing errors.
Independent consultant Basu and Friedli, a professor at the University of St. Gallen, reviewed a new systems-based approach to quality metrics in their article, following the university receiving a U.S. Food and Drug Administration (FDA) grant to undertake the effort. The goal is to recommend a measurement system based on St. Gallen’s Operational Excellence model, which encourages improved quality rather than lagging indicators that measure symptoms. The team, which also includes the Dublin Institute of Technology, stated that these new metrics will “help the FDA to establish a clear standard for review and inspection, allowing for a risk-based regulatory approach, transforming quality oversight from a qualitative to a quantitative risk-based process.”
For his part, Carlin, director of open innovation at FMC, warned that excipient risk cannot be fully assessed during development, as product and process changes, including scale-up, have the propensity to change the risk profile. Excipient criticality may be dependent on variations and process changes that occur during manufacturing, which will be unknown at the time of filing.
He added: “Continuous monitoring of impact from all excipients throughout the lifecycle is more important than a one-off arbitrary binary classification during development. The importance of all attributes and parameters should be evaluated for impact, and re-evaluated as new information becomes available.”
Emphasizing the panel’s concern regarding the need to shift towards quality cultures and away from binary measures of product failure, Hussain, who is CEO at Insight Advice & Solutions LLC, stated that the “file first, figure it out later” mindset is a fundamental part of the problem. He believes that companies that implement quality by design (also referred to as QbD) and process analytical technology (PAT) approaches early in development will see the greatest benefits and have the capabilities to file first, adding, “Broader adoption of PAT-based continuous manufacturing system by brand and by a couple of major generic and CDMOs should be more prominently evident in the next three years.”
Hussain believes the industry is now at a “tipping point” with the first adopters of continuous processing having been included in NDAs, and an excellent opportunity now exists for the manufacture of injectables and we should expect more progress over the next three years. However, he argued the ability to manufacture continuous, while significant, is, in fact, a business decision.
Similarly, Malhotra, who is president at EPCOT International, suggests that while there is much excitement around continuous processing, we must better define what it is we mean by “continuous” given that in terms of active pharmaceutical ingredients (APIs), very few products have the scale to be manufactured truly continuously. There simply aren’t the volumes needed, and the industry's greatest shortcoming is its overall record of manufacturing technology innovation.
As he noted, “All said and done, each company producing APIs or their formulations has to justify and use the most cost-efficient technology (batch, campaigned batch or continuous) to produce products that are economic and deliver the same quality all the time. Regulators can only regulate and assure product quality. They can suggest the technologies and methods companies should consider for their products. However, companies have to justify use of such technologies. Excellence comes from within the companies rather than outsiders.”
Summarizing the comments and insights before the Barcelona show in October, where they were set to be discussed, CPhI’s group director of pharma, Chris Kilbee, said, “[What] is clear is that whilst the industry is making significant improvements to overall quality, our experts believe that continuous improvement programs and ongoing analysis are more important to instilling a quality culture than simply striving to achieve minimum regulatory standards. What’s really exciting is that over the next few years we should see a shift towards harmonized standards and more advance manufacturing. By implementing the recommendations from our panel, the pharma industry will advance more quickly, develop better and safer drugs and realize the full potential of lower cost and higher-quality manufacturing.”
CPhI’s goal is to drive growth and innovation at every step of the global pharmaceutical supply chain, from drug discovery to finished dosage. Through exhibitions, conferences and online communities, CPhI brings together more than 100,000 pharmaceutical professionals each year to network, identify business opportunities and expand the global market. CPhI hosts events in Europe, Korea, China, India, Japan, Southeast Asia, Istanbul and Russia.

DDNews Staff

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