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5. The influence of clean room design on product contamination. Whyte W J Parenter Sci Technol; 1984; 38(3):103-8. PubMed ID: 6747777 [No Abstract] [Full Text] [Related]
6. Boundary and airlock design issues in aseptic facilities. Lorenz MR; Robinson JE J Parenter Sci Technol; 1991; 45(6):279-85. PubMed ID: 1802984 [TBL] [Abstract][Full Text] [Related]
7. Control of the aseptic processing environment. Frieben WR Am J Hosp Pharm; 1983 Nov; 40(11):1928-35. PubMed ID: 6650522 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Continuous microbiological air monitoring for aseptic filling lines. Ginsbury K PDA J Pharm Sci Technol; 2007; 61(4):225. PubMed ID: 17933205 [No Abstract] [Full Text] [Related]
10. Filling vials aseptically while monitoring for bacterial contamination. Dirksen JW; Larsen RV Am J Hosp Pharm; 1975 Oct; 32(10):1031-2. PubMed ID: 1190216 [TBL] [Abstract][Full Text] [Related]
11. Review of currently recommended aseptic procedures. I. Dental operatory contamination. Greenlee JS Dent Hyg (Chic); 1983 Nov; 57(11):22-7. PubMed ID: 6581084 [No Abstract] [Full Text] [Related]