# CPG Sec. 230.110-  Registration of Blood Banks, Other Firms Collecting, Manufacturing, Preparing or Processing Human Blood or Blood Products - FDA Guidance Document

Source: https://www.keypedia.com/guidances/compliance-policy-guide-cpg/cpg-sec-230110-registration-of-blood-banks-other-firms-collecting-manufacturing-preparing-or-processing-human-blood-or-blood-products/93e2ceb0-916e-420c-a653-ab3f1e7a6aae

> FDA guidance document: CPG Sec. 230.110-  Registration of Blood Banks, Other Firms Collecting, Manufacturing, Preparing or Processing Human Blood or Blood Products. Issue date: August 16, 2000. Get complete insights and analysis.

---

## Details

- Title: CPG Sec. 230.110-  Registration of Blood Banks, Other Firms Collecting, Manufacturing, Preparing or Processing Human Blood or Blood Products
- Communication Type: Compliance Policy Guide (CPG)
- Product Type: Biologics
- Office Name: Office of Regulatory Affairs
- Issue Date: 2000-08-16

## Related Documents

- [CPG Sec. 446.100 Regulatory Action Regarding Approved New Drugs and Antibiotic Drug Products Subjected to Additional Processing or other Manipulations](https://www.keypedia.com/guidances/compliance-policy-guide-cpg/cpg-sec-446100-regulatory-action-regarding-approved-new-drugs-and-antibiotic-drug-products-subjected-to-additional-processing-or-other-manipulations/835ffe14-080b-42e1-91af-560a4c342b5c)
- [CPG Sec. 398.300 Registration of Assemblers of  Diagnostic X-Ray Systems as Device Manufacturers](https://www.keypedia.com/guidances/compliance-policy-guide-cpg/cpg-sec-398300-registration-of-assemblers-of-diagnostic-x-ray-systems-as-device-manufacturers/6e914248-4106-463a-903e-980097243960)
- [CPG 230.120- Human Blood and Blood Products as Drugs](https://www.keypedia.com/guidances/compliance-policy-guide-cpg/cpg-230120-human-blood-and-blood-products-as-drugs/6ddcee95-2636-4d4a-91f0-d7f328e8f0ae)