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Products regulatory agency mhra - PowerPoint PPT Presentation

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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Drug Safety and Brexit

We provide cloud based software safety database solutions for pharmacovigilance which are not only cost effective and user friendly but also fully validated for quick, easy import, entry and electronic submissions of adverse event.

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Products regulatory agency mhra - PowerPoint PPT Presentation

e-Dossier Submission: Regulatory and Procedural Guidance

Drug Safety and Brexit