Regulatory agencies worldwide increasingly rely on standardized formats such as the electronic Common Technical Document (eCTD) for submissions to streamline the process for evaluating investigational drugs.
This has allowed for greater efficiency in submissions and reviews by improving clarity and consistency. And although using eCTD has made the process more efficient, getting documents in the proper format for submission is not always straightforward.
eCTD申請を成功させるために知っておきたいヒントとベストプラクティスを、当社の専門家がまとめました。
Inside this e-book:
- Why using the eCTD format is important
- What you need to know for a successful eCTD submission
- Answers to frequent eCTD questions
- Checklist for selecting a eCTD submission vendor
- … and more!
Simply complete the form to download your complete guide.
