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4. In vitro solubility studies of commercially available pharmaceutical products. Muti H; Papaioannou G; Choulis NH Pharmazie; 1983 Nov; 38(11):779. PubMed ID: 6669602 [No Abstract] [Full Text] [Related]
5. In vitro drug release rate as a standard requirement. Láng B Pharmazie; 1971 Nov; 26(11):661-4. PubMed ID: 5154319 [No Abstract] [Full Text] [Related]
6. Official USP Reference Standards: metrology concepts, overview, and scientific issues and opportunities. Williams RL; ; J Pharm Biomed Anal; 2006 Jan; 40(1):3-15. PubMed ID: 16303277 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Official inspections of a pharmaceutical plant during the registration of new products]. De Martiis F; Fontani F; Zanotti-Gerosa A Boll Chim Farm; 1982 Jul; 121(7):319-27. PubMed ID: 7150440 [No Abstract] [Full Text] [Related]
10. [Pharmacopoeias and official quality standards for pharmaceutical evaluation in the Hungarian People's Republic]. Laszlovszky J Pharmazie; 1981 Nov; 36(11):778-9. PubMed ID: 7323127 [No Abstract] [Full Text] [Related]
11. Conductimetric determination of phenylpropanolamine HCl, ranitidine HCl, hyoscyamine HBr and betaine HCl in their pure state and pharmaceutical preparations. Issa YM; Youssef AF; Mutair AA Farmaco; 2005; 60(6-7):541-6. PubMed ID: 15890349 [TBL] [Abstract][Full Text] [Related]
12. Safety pharmacology: an essential interface of pharmacology and toxicology in the non-clinical assessment of new pharmaceuticals. Claude JR; Claude N Toxicol Lett; 2004 Jun; 151(1):25-8. PubMed ID: 15177637 [TBL] [Abstract][Full Text] [Related]
13. [Problems of drug testing]. Zbinden G Schweiz Rundsch Med Prax; 1970 Jul; 59(28):1019-20. PubMed ID: 5512822 [No Abstract] [Full Text] [Related]
14. Biopharmaceutics and drug standards. Feldmann EG Am J Hosp Pharm; 1968 Mar; 25(3):111-9. PubMed ID: 5658858 [No Abstract] [Full Text] [Related]
15. Purpose and methodology in clinical trials on new drugs. Collins IS; Thorpe PC N Z Med J; 1970 Mar; 71(454):148-51. PubMed ID: 4910417 [No Abstract] [Full Text] [Related]
16. International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. IX. Recommendations on terms and symbols in quantitative pharmacology. Jenkinson DH; Barnard EA; Hoyer D; Humphrey PP; Leff P; Shankley NP Pharmacol Rev; 1995 Jun; 47(2):255-66. PubMed ID: 7568328 [No Abstract] [Full Text] [Related]
17. Biopharmaceutic equivalency and the role of the Food & Drug Administration. Hodges RM Am J Hosp Pharm; 1968 Mar; 25(3):121-7. PubMed ID: 5658859 [No Abstract] [Full Text] [Related]
18. [Problems of drug safety]. Liljestrand A Nord Med; 1967 Nov; 78(47):1535-9. PubMed ID: 6075272 [No Abstract] [Full Text] [Related]
19. Parenteral suspensions. Nash RA Bull Parenter Drug Assoc; 1972; 26(2):91-4. PubMed ID: 5012208 [No Abstract] [Full Text] [Related]
20. [Importance of dissolution profile in stability tests]. Lengyel M; Dredán J; Shafir G; Klebovich I; Antal I Acta Pharm Hung; 2007; 77(2):132-41. PubMed ID: 17933273 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]