Many of our readers will be familiar with our paper “Parallelism in Practice” (PDA Journal of Pharmaceutical Science and Technology, 2015) and how we examined the common methods... read more →
Following the EurPh recommendations mixes up system and sample suitability and can lead to undesirable results. Assays failing when they should pass Assays passing when they should fail We... read more →
We have previously discussed the 4 parameter logistic (4PL) model. Sometimes you may see slightly different versions of the 4PL equation – these are all mathematically equivalent. However,... read more →
Our recent paper, Estimation of Relative Potency from Bioassay Data that Include Values below the Limit of Quantitation (Francis Bursa, Kelly J. Fleetwood, Karie J. Hirst and Ann Yellowlees), discusses values... read more →
Previously, we discussed the definition of relative potency and how it relates to the concepts of biological similarity, and thus the need for parallelism between the reference dose response... read more →