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eCTD electronic filing to fulfill regulatory requirements

Thu, December 9th, 9:00 am – 10:30 am CST (China Standard Time)

GlobalSubmit™ software supports clinical studies and trials, marketing applications, and compliance with 21 CFR Part 11 specifications. It also integrates seamlessly with the industry’s leading electronic document management system (eDMS).
Streamlining the eCTD submission process will increase your efficiency, reduce risk, and ensure no technical rejections, and help your regulatory team submit all documents on time.

During our webinar, you will have the opportunity to interact with the speaker, and we will answer your questions.

**The webinar will be presented in English and Chinese.

Speakers

Marco Ding, Director of Business Development, Certara China
Guest speakers’ information is available on the registration page

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