A Short Course on Regulatory Affairs with emphasis on the Background, Content and Detail of Module 3 (PQMT_CTD3)
|Event Date/Time: Mar 24, 2010||End Date/Time: Mar 25, 2010|
AND WHO SHOULD ATTEND
This Course will be a comprehensive and group interactive course that builds from first principles and explores numerous pharmaceutical topics that have to be addressed in supporting documentation for Marketing Authorisation Applications (MAAs).
The course has been well developed over many years and has been highly regarded by delegates of varied experience in regulatory affairs and associated departments. Past delegates have been and future ones are expected to be from within the pharmaceutical and chemical industries (chemical development, analytical, formulation and pharmaceutical development, manufacturing, regulatory/registration departments) and the Competent Authorities (assessors, inspectors, scientific/medical writers).
The course is suitable for people new or relatively new to regulatory affairs, particularly people transferring within a company into product registration work, and for those needing a refresher course or an up-to-date understanding of CTD Module3.
Legacy Botleigh Grange Hotel & Spa, Southampton,