Abstract
In manufacturing settings, control limits are often set using a three-sigma rule (i.e., three estimated standard deviations above and below the estimated mean). More sophisticated statistical methods might include the use of confidence, prediction, or tolerance intervals. However, in environmental monitoring of microbial excursions in aseptic manufacturing operations, most of the assayed measurements fall below the limit of quantitation. In such circumstances, it is inappropriate to directly calculate control limits with a mean plus two or three standard deviations to represent the center and spread of the data. The system under consideration assumes that microbial assayed values stem from a log-normal distribution with two sources of variability to account for testing occasions and measurements made within a testing occasion. Bayesian statistical methods and a Tobit likelihood are used to model the observed and left-censored data in order to predict the distribution of new data. Control limits are generated from quantiles of the posterior predictive distribution.
- Received April 27, 2016.
- Accepted August 1, 2016.
- Copyright © 2016, Parenteral Drug Association