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Clean room microbiological evaluation

General Informational Chapter (1116) Microbiological Evaluation of Clean Rooms and Other Controlled Environments... [Pg.223]

USP 24 Testing Chapters (51) Antimicrobial Effectiveness Testing, (61) Microbial Limit Tests and (71) Sterility Tests, United States Pharmacopeial Convention, Inc., Rockville, MD, 2000. USP 24 Informational Chapters (1116) Microbiological Evaluation of Clean Rooms and other Controlled Environments, (1111) Microbiological Attributes of Pharmaceutical Articles, (1151) Pharmaceutical Dosage Forms, (1225) Validation of Compendial Methods, and (1231) Water for Pharmaceutical Purposes, United States Pharmacopeial Convention, Inc., Rockville, MD, 2000. [Pg.234]

General information <1116> Microbiological evaluation of clean rooms and other controlled environments. U.S. Pharmacopeia, vol. 25. Rockville, MD U.S. Pharmacopeial Convention, p. 2206-2212 (2002). [Pg.478]

Informational Chapters Microbiological Evaluation of Clean Rooms and Other Controlled Environments, Ch. 1116 Microbiological Attributes of Pharmaceutical Articles, Ch. 1111 Pharmaceutical Dosage Eorms, Ch. 1151 Validation of Compendial Methods, Ch. 1225 Water for Pharmaceutical Purposes, Ch. 1231. In U.S.P. 24. [Pg.2793]


See other pages where Clean room microbiological evaluation is mentioned: [Pg.222]    [Pg.223]    [Pg.2785]    [Pg.2785]    [Pg.259]    [Pg.259]   
See also in sourсe #XX -- [ Pg.223 ]




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