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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. しかし、適切な eCTD 閲覧ソフトウェアがなければ、単純かつ重要なレビュー作業が遅延し、棄却、コスト、ユーザーフラストレーションのリスクを増大させることになります。
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/
