e-Dossier Submission: Regulatory and Procedural Guidance
Taking out the paper blizzard associated with regulatory submissions through a process where applications are built up once from the start, and then handled over their lifecycle. It is an immense improvement over spending hours in a file room digging through files, taking out volume after volume just being able to pull up a 2-year-old investigational new drug (IND) application and look at it in a current view as well as a historical view in a few clicks. The secret to this significant change is the Popular Electronic Common Technical Document (eCTD), which represents a major advance in the global march towards electronic regulatory submissions. Learn More: http://bit.ly/2UrwyGV Need Help: Uk: 44- 7424810299 Email: sales@pepgra.com Whatsapp: 91 9884350006
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