Correlating Product Lifecycle and Manufacturing Site Characteristics with Critical-to-Quality Product Deviations

MIT survey results address product and site characteristics that statistically correlate with quality performance.

Although there is awareness among the biopharmceutical industry of the challenges and trade-offs associated with monitoring the safety of drug products, there does not seem to be a clear and consistent understanding of characteristics correlated with the presence of critical-to-quality deviations of a product at the commercial scale (1). The intent of this paper is to initiate an understanding of product and site characteristics that statistically correlate with quality performance of biopharmaceutical commercial products. Towards this objective, a comprehensive survey on related topics is underway at the Massachusetts Institute of Technology (MIT) Center for Biomedical Innovation (CBI). The interim results described in this research represent survey results from 34 commercial-scale biopharmaceutical products at 11 international sites. This research builds on analysis done by the MIT CBI team earlier this year (2).

Some regulatory agencies, including FDA, have actively pursued a risk-based approach to manufacturing site inspection because their inspections are site-specific and not restricted to an individual product (1). Explicit inputs that FDA uses for its risk-based selection of sites to inspect include the types of products manufactured (e.g., prescription versus over-the-counter, approved versus unapproved, therapeutic classes); the control and/or contamination potential of the manufacturing environment (e.g., facility size, facility type, number of drug products, sterility requirements); and cost of inspection (e.g., domestic versus international locations). These inputs are logical for consideration of total risk to quality at the level of a site, but, in this research, the focus regarding quality is on the product.

Survey methodology

A comprehensive survey on topics related to site characteristics, quality approaches, quality activities, perception of relative consistency of regulators, product-level process details, and product-level compliance performance has been developed by MIT's CBI. The survey includes questions that result in a total of 57 variables across these topic areas. The developed survey was tested with industry representatives and then deployed over the past 18 months as a secure web-based questionnaire directly to biopharmaceutical manufacturing sites through several different channels. The individuals targeted for inclusion as survey respondents have been manufacturing plant managers or their representatives.

In total, 20 sites representing 52 manufactured products have completed the survey. These responses have been filtered to focus on commercial-scale manufacturing and products for which all relevant information was provided. This reduced the number of products included thus far to 34 across 11 sites.

The research is supported by the Alfred P. Sloan Foundation of New York City.