MEETINGS - Intensive course on Current Good Manufacturing Practice for the Pharmaceutical and Medical Device Industries (the Netherlands) September 2003:
This article was originally published in Clinica
Executive Summary
A three-day intensive course on Current Good Manufacturing Practice (CGMP) for the Pharmaceutical and Medical Device Industries will take place on September 3-5 2003 at the Radisson SAS Hotel, Amsterdam, The Netherlands. The event focuses on understanding CGMP regulations including document requirements, quality systems, monitoring practices and management responsibility. It will also focus on the elements of an FDA inspection and how it compares to those of other regulatory systems. Further details from The Center for Professional Development, on tel: +31 20 638 28 06; fax: +31 20 620 21 36 www. cfpa.com