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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. 问题是，如果没有合适的 eCTD 阅读软件，简单但关键的审阅任务就会造成延迟，增加被拒绝的风险、成本和用户受挫感。
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/
