21 CFR Part 11 Course at ISPE 2010 Philadelphia Training EventCourse features latest information on the status of FDA’s current reexamination
Tue, 11/02/2010 - 10:49
(ISPE, Tampa, FL) -- ISPE, a global not-for-profit association of 22,000 pharmaceutical science and manufacturing professionals, will offer seven training courses, including a session focused on complying with 21 CFR Part 11, at its 2010 ISPE… Product Quality Life-Cycle Implementation GuideFirst in a how-to series to help develop and implement pragmatic approaches to product realization
Mon, 10/25/2010 - 13:04
(ISPE: Tampa, FL) -- ISPE, a global not-for-profit association of 22,000 pharmaceutical science and manufacturing professionals, has released a new good practice guide (GPG) titled Product Quality Lifecycle Implementation (PQLI) Guide: Overview of… Event: FDA-ISPE Collaboration: Pharmaceutical Quality SystemsEvent to focus on pharmaceutical quality systems.
Fri, 05/07/2010 - 10:41
(ISPE: Tampa, FL) -- The International Society for Pharmaceutical Engineering (ISPE), a global nonprofit association of 24,000 pharmaceutical science and manufacturing professionals, and the U.S. Food and Drug Administration (FDA) are co-sponsoring… Reshaping Pharmaceutical Quality
Tue, 06/10/2008 - 22:00
(ISPE: Tampa, Florida) -- The June 2008 issue of the Journal of Pharmaceutical Innovation (JPI) is publishing the first scientific papers outlining the progress made on the International Society for Pharmaceutical Engineering’s (ISPE) product… ISPE Releases Guide on Electronic Records and Signatures Good Practices
Tue, 04/26/2005 - 22:00
(ISPE: Tampa, FL) -- The International Society for Pharmaceutical Engineering (ISPE) announced the availability of its newest technical publication, “GAMP Good Practices Guide: A Risk-Based Approach to Compliant Electronic Records and Signatures.”…
