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7. Carrying out biological qualification, the control operation of moist-heat (steam sterilization) processes for producing sterile pharmaceuticals and medical devices. Pflug IJ; Evans KD PDA J Pharm Sci Technol; 2000; 54(2):117-35. PubMed ID: 10822983 [TBL] [Abstract][Full Text] [Related]
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16. Evaluation of Bacillus oleronius as a Biological Indicator for Terminal Sterilization of Large-Volume Parenterals. Izumi M; Fujifuru M; Okada A; Takai K; Takahashi K; Udagawa T; Miyake M; Naruyama S; Tokuda H; Nishioka G; Yoden H; Aoki M PDA J Pharm Sci Technol; 2016; 70(1):30-8. PubMed ID: 26889054 [TBL] [Abstract][Full Text] [Related]
17. Development and evaluation of a laboratory-scale apparatus to simulate the scale-up of a sterile semisolid and effects of manufacturing parameters on product viscosity. Chu PI; Doyle D Pharm Dev Technol; 1999; 4(4):553-9. PubMed ID: 10578510 [TBL] [Abstract][Full Text] [Related]
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19. Determining the capability of a drug product to be terminally sterilized: a case study involving a heat-sensitive, oxygen-sensitive drug product. Duncan MR; Wang PL; Moldenhauer JE Pharm Dev Technol; 1998 Nov; 3(4):527-34. PubMed ID: 9834956 [TBL] [Abstract][Full Text] [Related]
20. Impact of terminal heat sterilization on the quality of peritoneal dialysis solutions. Martis L; Henderson LW Blood Purif; 1997; 15(1):54-60. PubMed ID: 9096907 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]