# Biological Products: Reporting of Biological Product Deviations in Manufacturing
> **Food and Drug Administration** · Final rule. · Published 2000-11-07 · Effective 2000-05-07 · 65 FR 66621
## Document
- **Document number:** 00-28133
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 65 FR 66621
- **CFR reference:** 21 CFR 600
- **Publication date:** 2000-11-07
- **Effective date:** 2000-05-07
- **HHS docket:** Docket No. 97N-0242
## Abstract

The Food and Drug Administration (FDA) is amending the regulation requiring licensed manufacturers of biological products to report errors and accidents in manufacturing that may affect the safety, purity, or potency of a product. FDA also is amending the current good manufacturing practice (CGMP) regulations for blood and blood components to require establishments involved in the manufacture of blood and blood components, including licensed manufacturers, unlicensed registered establishments and transfusion services, to report biological product deviations in manufacturing. The final rule requires licensed manufacturers, unlicensed registered blood establishments, and transfusion services who had control over the product when a deviation occurred to report to FDA the biological product deviation if the product has been distributed. The final rule also establishes a 45-day reporting period. FDA is issuing the final rule as part of a retrospective review under Executive Order 12866 of significant FDA regulations to improve the effectiveness of FDA's regulatory program.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2000/11/07/00-28133/biological-products-reporting-of-biological-product-deviations-in-manufacturing)
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