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22. [Quality control of infusion fluids. II. Quantitative analysis of infusion fluids]. van den Bemd AA Pharm Weekbl; 1970 Jan; 105(4):97-9. PubMed ID: 5417757 [No Abstract] [Full Text] [Related]
32. Studies on microbiological contamination of in-use IV-fluids. Stjernström G; Gunnarsson B; Wikner H Acta Pharm Suec; 1978; 15(3):169-74. PubMed ID: 362822 [No Abstract] [Full Text] [Related]
33. Hygienic standard of parenteral solutions. Winding O Ugeskr Laeger; 1977 Dec; 139(49):2940-4. PubMed ID: 595183 [No Abstract] [Full Text] [Related]
34. Design control and validation of a facility for sterile clinical trial preparations. Staines L J Parenter Sci Technol; 1984; 38(3):109-14. PubMed ID: 6747778 [No Abstract] [Full Text] [Related]
35. Structure of products prepared by freeze-drying solutions containing organic solvents. Seager H; Taskis CB; Syrop M; Lee TJ J Parenter Sci Technol; 1985; 39(4):161-79. PubMed ID: 4032158 [No Abstract] [Full Text] [Related]
36. Letter: Addition of drugs to intravenous fluids. Lancet; 1976 Apr; 1(7964):858. PubMed ID: 56671 [No Abstract] [Full Text] [Related]
38. [Reliability of infusion systems and equipment]. Schmitz JE; Schreiber MN Klin Anasthesiol Intensivther; 1990; 38():274-88. PubMed ID: 2232611 [No Abstract] [Full Text] [Related]
39. Application of the Limulus amebocyte lysate assay in outbreaks of pyrogenic reactions associated with parenteral fluids and medical devices. Highsmith AK; Anderson RL; Allen JR Prog Clin Biol Res; 1982; 93():287-99. PubMed ID: 7122595 [No Abstract] [Full Text] [Related]
40. In-use physicochemical and microbiological stability of biological parenteral products. Ricci MS; Frazier M; Moore J; Cromwell M; Galush WJ; Patel AR; Adler M; Altenburger U; Grauschopf U; Goldbach P; Fast JL; Krämer I; Mahler HC Am J Health Syst Pharm; 2015 Mar; 72(5):396-407. PubMed ID: 25694415 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]