NSF/ANSI 455-4 : 2018
Superseded
View Superseded by
Good Manufacturing Practices for Over-the-Counter Drugs
English
12-11-2018
12-14-2020
This Standard is intended to define a standardized approach for auditing to determine the level of compliance of over-the-counter (OTC) drug products to 21 CFR Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General and 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals, well as incorporating additional retailer requirements.
| DocumentType |
Standard
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| Pages |
44
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| ProductNote |
This Standard also refers to 21 CFR § 211.22,21 CFR Part 11,21 CFR § 211.100,21 CFR § 211.101,21 CFR § 211.103,21 CFR § 211.110,21 CFR § 211.111,21 CFR § 211.115,21 CFR § 211.122,21 CFR § 211.122,21 CFR § 211.125,21 CFR § 211.130,21 CFR § 211.132,21 CFR § 211.134,21 CFR § 211.137,21 CFR § 211.142,21 CFR § 211.150,21 CFR § 211.160,21 CFR § 211.165,21 CFR § 211.166,21 CFR § 211.167,21 CFR § 211.170,21 CFR § 211.180,21 CFR § 211.182,21 CFR § 211.184,21 CFR § 211.188,21 CFR § 211.192,21 CFR § 211.196,21 CFR § 211.198,21 CFR § 211.204,21 CFR § 211.208,21 CFR § 211.25,21 CFR § 211.28,21 CFR § 211.34,21 CFR § 211.42,21 CFR § 211.44,21 CFR § 211.48,21 CFR § 211.50,21 CFR § 211.52,21 CFR § 211.56,21 CFR § 211.58,21 CFR § 211.63,21 CFR § 211.65,21 CFR § 211.67,21 CFR § 211.68,21 CFR § 211.80,21 CFR § 211.84,21 CFR § 211.86,21 CFR § 211.89,21 CFR § 211.94,21 CFR Part 7 Subpart C,
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| PublisherName |
NSF International
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| Status |
Superseded
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| SupersededBy |
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