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 the 23rd DIA Japan Annual Workshop for Clinical Data 2020-2025

2020-2025 Form

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we are in front of a new legal framework this new regulation it's really a challenge and it brings a new clinical trial information system a new platform that brings all functionalities or which you need to communicate with member states this Workshop it's really the main objective it's to support sponsors and all other attendees that would like to understand on how to properly uh populate and prepare a package to make the submission into CIS part one and part two it's really important to understand that the quality of these packages so the way we are preparing these packages it's critical and this can even avoid some considerations at the validation step the way we prepare these packages it's really critical if you want to avoid to have withdrawal or lapses in your trials so I really recommend you to come to this Workshop to learn a little bit to understand what type of documents should be submitted what are the main rules how things sho

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