Analyzing the Potency and Stability of Bioassays

This webinar is in English, 11:00 a.m. US Eastern Time (16:00 BST).

Learn how to use JMP to analyze biological assays during pharmaceutical and biotechnology development to help prepare for regulatory submissions, develop standard operating procedures and maintain good manufacturing practices. See how to use build and analyze parallelism between a pair of doses and responses, estimate relative potency, determine when a drug dose or concentration reaches toxicity, determine the affinity of the enzyme to the substrate, identify the 50% dose concentration (EC50) necessary to cause half of the maximum possible effect, and determine equivalence of different formulations.

This webinar covers: Fitting non-linear models, Parallelism Tests, Relative Potency Estimates, Equivalence Tests, Inverse Prediction for EC50 and IC50, and estimating Vmax and Km.