Event Date/Time: Nov 18, 2009 | End Date/Time: Nov 20, 2009 |
Description
• Receive updates on global regulatory environments and how they impact the access of medicines and future research and development in the region
• Discussions will highlight the benefits, barriers, and direction of harmonization and regulatory trends across the development lifecycle
Sessions include:
• Current Status of Pan American Network for Drug Regulatory Harmonization (PANDRH): Overview and Working Group
• Good Regulatory Practice (GRP): Ensuring Quality Throughout the Regulatory Process
• Collaborative Efforts on Inspections
• Collaborative Efforts on Pharmacovigilance
• Global Clinical Development: Opportunities in Latin America
• Biotechnology Paradigm in Latin America
• Promoting Faster Access by Globalizing Regulatory Processes
• Much more!
Simultaneous English/Spanish Translation Available
Hear from Experts Representing:
AMEIFAC, Mexico; CENCEC, Cuba; INAME, Argentina;
Center for Drug Evaluation and Research, FDA, USA; PhRMA, USA; OCA Hospital / Monterrey International Research Center, Mexico; Health Canada; Boehringer Ingelheim Mexico; Centre for Medicines Research International, UK; Universidad San MartÃn de Porres, Peru; Instituto Nacional de Higiene Rafel Rangel. Venezuela; Office of the Commissioner, FDA, US; CECMED, Cuba; Parexel, Argentina; Covance Inc., Mexico; and many more!
Conference Information:
USA: Ellen Diegel, Program Manager
Phone: 215-442-6158, Fax: (215) 293-5965
Email: ellen.diegel@diahome.org
Registration and Hotel:
B.P. Servimed, S.A. De C.V.
Email: dia@servimed.com.mx
Register Online:
http://www.servimed.com.mx/DIA09/indexi.htm