2025 年 6 月 25 日
常见问题解答
When will the FDA release ESGNG for the pharmaceutical and biotech industry?
ESG NextGen is currently available effective 2025 年 4 月 14 日.
How do I register a new account for FDA ESG NextGen?
Understanding the two entities in ESGNG will help answer this question best for your situation. The two entities are Company and Agency.
- A Company is a US or international business entity that uses ESGNG to file required regulatory or voluntary submissions to the FDA.
- An Agency can be a Contract Research Organization (CRO), a U.S. agent company (a liaison that ensures proper and timely communication between the FDA and a foreign pharmaceutical company), or a consulting company.
Identifying which entity applies to you is key to completing the registration process correctly. If you are an agency, you must obtain and upload a letter authorizing you to submit on behalf of a company. This letter of authorization (LOA) needs to be uploaded for every company you work for before you can complete any submissions on their behalf.
A non-repudiation letter (NRL) is also required and certifies electronic signatures. A companywide NRL or an individual NRL is acceptable.
Can I continue to use WebTrader when ESGNG goes live?
No. FDA plans to retire WebTrader and will only accept submission packages using ESGNG starting April 14.
Can I continue to use ESGNG for submissions to Health Canada?
可以。ESGNG functions in the same manner as using WebTrader for eCTD submissions to Health Canada.

Read our white paper for the tips and best practices you need to know for a successful eCTD submission.

Senior Regulatory Operations Specialist
Carrie Ngangnang is a Senior Regulatory Operations Specialist with several years of experience in regulatory operations electronic publishing, serving as project lead on multiple application types and over 20 years serving in leadership roles, managing people and projects ranging from few to 300+ stakeholders.
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