Stability Testing for Drug Substances and Drug Products 25-26 November 2008 Copenhagen, Demark Please click here to view the program of this conference or course To book for this program, just click on the option: Book this option: Non-ECA Members (EUR 1290,--) Book this option: ECA Members (EUR 1161,--) Book this option: EU GMP Inspectorates (EUR 645,--) Book this option: APIC Members (does not include ECA membership) (EUR 1225,--)
At this conference we offer a Conference Exhibition. Please click here in order to view the registration form (PDF) for exhibitors.
Objectives This event is intended to provide information on different aspects of stability testing. The conference will be opened by an overview of stability testing with a special focus on important changes in current revisions of ICH Guidelines. In the subsequent presentations, practical aspects of stability testing for drug substances and throughout drug development are discussed. The second day commences with a lecture on stability testing for Drug Products and a risk based approach for stability testing covering different climatic zones. In the following talks special consideration is given to the various aspects of post-marketing stability testing procedures. The specific challenges of data evaluation and the structure of the Common Technical Document (CTD) will then be addressed. The conference is rounded off by a presentation on stability testing of biological and biotechnological products.