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3. Statistical characteristics of the USP content uniformity test. Pedersen AO; Torud Y Pharm Acta Helv; 1971 Feb; 46(2):114-20. PubMed ID: 5142661 [No Abstract] [Full Text] [Related]
4. Content uniformity acceptance limit for a validation batch--suppositories, transdermal systems, and inhalations. Senderak ET Drug Dev Ind Pharm; 2009 Jun; 35(6):735-7. PubMed ID: 19514989 [TBL] [Abstract][Full Text] [Related]
5. The USP content uniformity test. Analysis and proposals. Setnikar I Pharm Acta Helv; 1974; 49(9-10):302-8. PubMed ID: 4462139 [No Abstract] [Full Text] [Related]
6. Panel discussion: proposed changes in the USP--microbiological aspects. I. Proposed changes in the USP sterility test. Clapp FL Bull Parenter Drug Assoc; 1969; 23(6):252-4. PubMed ID: 4901566 [No Abstract] [Full Text] [Related]
7. USP standards. Banes D Am J Hosp Pharm; 1976 Dec; 33(12):1245. PubMed ID: 998641 [No Abstract] [Full Text] [Related]
8. An epic decision by USP. Provost GP J Am Pharm Assoc; 1977 Sep; 17(9):547. PubMed ID: 893923 [No Abstract] [Full Text] [Related]
9. Relationship of USP-NF to NDA and ANDA "Standards". Belson JJ Am J Hosp Pharm; 1982 May; 39(5):869-70. PubMed ID: 7081269 [No Abstract] [Full Text] [Related]
10. USP and the Drug Regulation Reform Act. Heller WM J Parenter Drug Assoc; 1979; 33(2):55-60. PubMed ID: 255147 [No Abstract] [Full Text] [Related]
11. USP standards for dissolution and bioavailability. Grady LT Am J Hosp Pharm; 1982 Sep; 39(9):1546-8. PubMed ID: 7137198 [No Abstract] [Full Text] [Related]
12. Voluntary standards--the USP and the PDA. Schmitz AJ J Parenter Drug Assoc; 1980; 34(6):425-6. PubMed ID: 6906364 [No Abstract] [Full Text] [Related]
13. General requirements for parenteral pharmaceuticals for the 21st USP revision--for the 21st Century. Barnstein CH J Parenter Drug Assoc; 1979; 33(5):287-9. PubMed ID: 259651 [No Abstract] [Full Text] [Related]
15. USP--promoting the public health. Carothers N Todays Surg Nurse; 1998; 20(1):35-9. PubMed ID: 9866636 [TBL] [Abstract][Full Text] [Related]
16. Content uniformity and assay requirements in current regulations. Bánfai B; Ganzler K; Kemény S J Chromatogr A; 2007 Jul; 1156(1-2):206-12. PubMed ID: 17109871 [TBL] [Abstract][Full Text] [Related]
17. The potential impact of usp general chapter <797> on procedures and requirements for the preparation of sterile radiopharmaceuticals. Hung JC J Nucl Med; 2004 Jun; 45(6):21N-6N. PubMed ID: 15181115 [No Abstract] [Full Text] [Related]