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4. Viability-based rapid microbiological methods for sterility testing and the need for identification of contamination. Moldenhauer J. PDA J Pharm Sci Technol; 2006; 60(2):81-8. PubMed ID: 16696190 [No Abstract] [Full Text] [Related]
5. Introduction to papers on mycoplasmology presented at a Parenteral Drug Association mycoplasma workshop. Potts BJ. Biologicals; 2010 Mar; 38(2):181-2. PubMed ID: 20079662 [No Abstract] [Full Text] [Related]
10. The influence of clean room design on product contamination. Whyte W. J Parenter Sci Technol; 1984 Mar; 38(3):103-8. PubMed ID: 6747777 [No Abstract] [Full Text] [Related]
11. Design control and validation of a facility for sterile clinical trial preparations. Staines L. J Parenter Sci Technol; 1984 Mar; 38(3):109-14. PubMed ID: 6747778 [No Abstract] [Full Text] [Related]
12. An approach to establishing parenteral solution sterilization cycles. Korczynski MS, Peterson CL, Loshbaugh CC. Bull Parenter Drug Assoc; 1974 Mar; 28(6):270-7. PubMed ID: 4455323 [No Abstract] [Full Text] [Related]
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15. The incubation period in sterility testing. Bathgate H, Lazzari D, Cameron H, McKay D. J Parenter Sci Technol; 1993 Mar; 47(5):254-7. PubMed ID: 8263662 [Abstract] [Full Text] [Related]
16. Current practices in endotoxin and pyrogen testing in biotechnology. The Quality Assurance/Quality Control Task Group. Parenteral Drug Association. J Parenter Sci Technol; 1990 Mar; 44(1):39-45. PubMed ID: 2313492 [Abstract] [Full Text] [Related]
17. Sterility-testing program for antibiotics and other intravenous admixtures. Choy FN, Lamy PP, Burkhart VD, Tenney JH. Am J Hosp Pharm; 1982 Mar; 39(3):452-6. PubMed ID: 7041640 [No Abstract] [Full Text] [Related]