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Code of Federal Regulations
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Title 21
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Chapter I — Food and Drug Administration, Department of Health and Human Services
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Subchapter C — Drugs: General
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Part 230 — Certification and Postmarketing Reporting for Designated Medical Gases
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Pt. 226
Current Good Manufacturing Practice for Type a Medicated Articles
Pt. 250
Special Requirements for Specific Human Drugs
›
Part 230 — Certification and Postmarketing Reporting for Designated Medical Gases
Search Part 230 full text →
Subpt. A
General Provisions
§§230.1 to 230.3
Subpt. B
Certification of Designated Medical Gases
§§230.50 to 230.150
Subpt. C
Postmarketing Quality and Safety Reporting
§§230.205 to 230.230
‹
Pt. 226
Current Good Manufacturing Practice for Type a Medicated Articles
Pt. 250
Special Requirements for Specific Human Drugs
›
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