# Providing Regulatory Submissions in Electronic Format--Submission of Manufacturing Establishment Information Guidance for Industry - FDA Guidance Document

Source: https://www.keypedia.com/guidances/guidance-document/providing-regulatory-submissions-in-electronic-format-submission-of-manufacturing-establishment-information-guidance-for-industry/0221e8af-59ae-437d-88f1-5504fb12c147

> FDA guidance document: Providing Regulatory Submissions in Electronic Format--Submission of Manufacturing Establishment Information Guidance for Industry. Issue date: July 23, 2019. Get complete insights and analysis.

---

## Details

- Title: Providing Regulatory Submissions in Electronic Format--Submission of Manufacturing Establishment Information Guidance for Industry
- Communication Type: Guidance Document
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research
- Issue Date: 2019-07-23

## Related Documents

- [Assessing User Fees Under the Generic Drug User Fee Amendments of 2017 Guidance for Industry](https://www.keypedia.com/guidances/guidance-document/assessing-user-fees-under-the-generic-drug-user-fee-amendments-of-2017-guidance-for-industry/15016857-1152-47bd-87a5-412d726e1dfc)
- [Study and Evaluation of Sex Differences in the Clinical Evaluation of Drugs:  Guidance for Industry](https://www.keypedia.com/guidances/guidance-document/study-and-evaluation-of-sex-differences-in-the-clinical-evaluation-of-drugs-guidance-for-industry/3a0ffb0a-7a37-4bc1-87ac-ca6b3fb05058)
- [Limiting the Use of Certain Phthalates as Excipients in CDER-Regulated Products:  Guidance for Industry](https://www.keypedia.com/guidances/guidance-document/limiting-the-use-of-certain-phthalates-as-excipients-in-cder-regulated-products-guidance-for-industry/3781a274-d4b8-4b5c-b800-79fcdaac4674)