Event Date/Time: Apr 10, 2003
End Date/Time: Apr 11, 2003
Many organizations have already implemented eSubmissions programs and since 1998,the average number of voluntary electronic NDAs submitted per month to the FDA has consistently doubled. This training course provides tools to facilitate the transition to an electronic environment. The program is essential for individuals embarking on or considering electronic submission programs. Attendees evaluate the benefits of electronic publishing solutions and gain tips for implementation and trouble-shooting. Implement best practices and reduce time to publish and deliver regulatory submissions. Achieve simultaneous global submissions from a set of common source files. Analyze solutions for implementing document management systems and ensuring integration with publishing and other systems. Participate in this highly interactive course that prepares attendees to overcome the vast challenges ahead by interpreting the guidances, clarifying requirements and evaluating routes of implementation.