Leading Industry body DIA (Drug Information Association is organizing a day long eCTD training workshop for pharma professionals on February 4 in Mumbai. This workshop is focused on enabling the participants to compile, publish and validate eCTD submissions with insights on Life Cycle Management and STF compilations.
Hands-on training will enable participants to understand regional differences and global submission strategies. Compilation of US M1 and EU M1 will be discussed in detail to empower users with updated information on these major ICH regions. This course is designed for anyone pursuing or intending to pursue Regulatory Affairs, Regulatory Operations, Submissions Management and Electronic Publishing.
An interactive presentation will be also given by LORENZ Life Sciences' Professional Services Director, Kent Briggs, who will highlight the latest eCTD activities on a global scale. Attendees will also consider the impact of regional interpretations of eCTD specifications and guidelines on global submissions strategy.
