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Your organization has numerous stakeholders responsible for reviewing the content of your drug submissions which requires approving eCTD submission content quickly, fielding agency questions on the fly, and often entails referencing in-stream as well as historical submissions to do so. The trouble is, without the right eCTD viewing software in place, simple yet critical review tasks can cause delays, increasing your risk of rejection, costs, and user frustration.
Attend this webinar to learn how Certara’s GlobalSubmit WebReview eCTD viewer facilitates a fast, efficient, and dynamic regulatory review of your submissions. Cloud-hosted and web-based, GlobalSubmit WebReview eCTD software has been tested and validated with some of the largest applications received by Health Authorities. For more information on GlobalSubmit Webreview eCTD viewer, please visit: certara.com/globalsubmit-webreview/