ISSN: 2329-6631
+44 1478 350008
Alan Liss
GXP Farma, LLC�Consulting, USA
Posters & Accepted Abstracts: J Develop Drugs
Global pharmaceutical trends confirm the importance of Asian pharmaceutical manufacturing facilities as the most critical aspect of maintaining the supply of many of the drugs currently on the market. However, recurring issues in regard to product quality and general compliance to established quality standards put a potential cloud over the otherwise bright future of this region of the pharma world. This presentation shall summarize information gained while a member of US FDA and as a current subject matter expert in Asia regarding current, present and future compliance to regulatory standards in key Asian markets. Data emphasis will be on small molecule generics but with a critical evaluation of the future of biosimilars produced in these same areas. The connection between pharmaceutical standards and cultural norms will be made and how these will affect the future of manufacturing in Asia, specifically and the global pharmaceutical supply chain in general.
Email: lissnest@yahoo.com