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Manufacturing Quality: part one of a three-part series
March 2, 2022
By: TOM BRANNA
Chief Content Officer
This is the first of a three-part series that describes and details the role and function of a central element of manufacturing quality—the manufacturing plant hygienist. By Philip Geis, PhD, Geis Microbiological Quality affiliated with Advanced Testing Laboratory • Deepika Raina, L’Oreal • Geoff Waby, Advanced Testing Laboratory • Michael Loewenstein, Q Laboratories LLC • Pamela Wilger, Cargill Inc. Manufacturing Hygiene Task Force, PCPC Microbiology & Quality Committees The mid to late-20th Century found substantial compromises in microbiological quality of personal care products.1 Testing of marketed products in the US and Europe found concerning numbers of contaminated products. The personal care industry’s very effective response through the 70’s and 80’s included development of more effective preservatives and improved manufacturing quality. The success of this effort was recognized by the FDA as the 20th Century closed.2 Unfortunately, this 20th Century combination of preservation and manufacturing quality has not been maintained. Although effective and considered safe-in-use by relevant health authorities, traditional preservatives have fallen into marketing disfavor leading many to formulate with alternative preservative systems. Preservation is primarily intended to protect consumers in use. Manufacturing hygiene has not been optimized to its potential. It was not considered as a critical parameter by management. Preservatives were heavily relied on to protect the end-use products and in some ways to mitigate poor practices in the manufacturing process. Significant microbiological issues have resurfaced in the 21st Century in context of alternative systems. Due to consumer pressure and a desire for non-traditional preservatives, the explosion of alternative preservative systems such as multifunctional ingredients and organic acids, saw increased use in the personal care market. The problem is especially impacting mid- to smaller-sized manufacturers. Regulatory publication and enforcement reports find a significant number of incidents of microbiological contamination of cosmetics associated with alternative systems.3 Reasonably, these reports find alternative systems in their secondary role inadequate to support relevant non-sterile manufacturing systems. Labels indicate major manufacturers have largely maintained traditional preservations and are not included in contamination reports. However, they too are under marketing pressure. Microbiological Quality with Alternative Systems
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