# Electronic Drug Product Reporting for Human Drug Compounding Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act” - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/electronic-drug-product-reporting-for-human-drug-compounding-outsourcing-facilities-under-section-503b-of-the-federal-food-drug-and-cosmetic-act/663cef2e-7472-423d-8bba-249d7de0ea3d

> FDA guidance document: Electronic Drug Product Reporting for Human Drug Compounding Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act”. Issue date: January 03, 2017. Get complete insights and analysis.

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## Details

- Title: Electronic Drug Product Reporting for Human Drug Compounding Outsourcing Facilities Under Section 503B of the Federal Food, Drug, and Cosmetic Act”
- Communication Type: Guidance Document
- Product Type: drugs
- Office Name: Center for Drug Evaluation and Research
- Office URL: /offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
- Issue Date: 2017-01-03
- Last Changed: 2022-04-28
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2013-N-1428">FDA-2013-N-1428</a>

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