From: Tuesday, September 21, 2010
To: Thursday, September 23, 2010
Venue:
Hilton Woodbridge, Iselin, NJ, USA
Agenda:
This three-day course is designed for clinical supplies and regulatory affairs professionals such as project managers, supervisors, technicians, and QA/QC associates. The course includes topics on phases of new drug development, documentation requirements, clinical protocol interpretation, clinical supplies life cycle, and outsourcing best practices.
For more information, please contact Sarah Nackson at 908-233-4508 or snackson@jeiven.com.
