Drug Stability, Third Edition, Revised, and Expanded: Principles and Practices
Drug Stability, Third Edition, Revised, and Expanded: Principles and Practices By Carstensen, Jens T.
2000 | 792 Pages | ISBN: 0824703766 | PDF | 30 MB
2000 | 792 Pages | ISBN: 0824703766 | PDF | 30 MB
Everything made by human hands—from the sublime Parthenon to the trivial milkshake—is subject to decay. Pharmaceuticals are no exception to this general statement. If there is any functionally relevant quality attribute of a drug product that changes with time, evaluation of this change falls within the purview of the pharmaceutical scientists and regulators who quantify drug product stability and shelf life. Describing the documentation required to minimize the changes of regulatory citations, the book lists manufacturers of photostability testing chambers, stability system software, and laboratory information management systems for pharmaceutical applications.