Watch the On-Demand Webinar
As the FDA rolls out ESG NextGen to modernize how it securely receives and processes electronic submissions, including new options such as a web-based Unified Submission Portal (USP), API-based submissions, and AS2 connectivity, regulatory teams need submission operations that can keep up.
In this on-demand webinar, you’ll see how Certara’s GlobalSubmit™ helps you capitalize on ESG NextGen by streamlining the work before you hit “send”: publishing submission-ready eCTD content, running robust validation to catch compliance issues early, and enabling efficient, collaborative review so your packages are ready for transmission via ESG NextGen’s USP/API/AS2 pathways.
What You’ll Learn
- How the FDA ESG NextGen API enables faster, automated regulatory submissions
- Ways automation reduces errors, lowers costs, and improves team efficiency
- What modern ESG integration looks like and how to get started
This webinar is ideal for:
This webinar is for regulatory and submission professionals involved in preparing, publishing, validating, or managing FDA electronic submissions, especially those planning for or transitioning to ESG NextGen.
It’s ideal for Regulatory Operations, Regulatory Affairs, submission publishing, regulatory IT, quality/compliance, and biopharma or CRO teams responsible for eCTD readiness and submission workflows.
