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35. PDA comments on USP in-process revision <1116> microbiological evaluation of clean rooms and other controlled environments. Parenteral Drug Association. PDA J Pharm Sci Technol; 1995; 49(6):264-6. PubMed ID: 8581456 [TBL] [Abstract][Full Text] [Related]
36. PDA's response to FDA's "Guideline on sterile drug products produced by aseptic processing". Akers JE; Agalloco JP; Carleton FJ; Korczynski MS J Parenter Sci Technol; 1988; 42(4):114-7. PubMed ID: 3183865 [No Abstract] [Full Text] [Related]
37. Questions on sterile technique can lead to study and research. Martin M Can Oper Room Nurs J; 1992; 10(2):19-21. PubMed ID: 1623437 [No Abstract] [Full Text] [Related]
38. Research: theory development in nursing. Zalar MK Perioper Nurs Q; 1986 Mar; 2(1):77-81. PubMed ID: 3639505 [No Abstract] [Full Text] [Related]
39. Control aspects of aseptically produced products. Avallone HL J Parenter Sci Technol; 1985; 39(2):75-9. PubMed ID: 3989616 [No Abstract] [Full Text] [Related]
40. Principles of aseptic technique. Oliver W Can Oper Room Nurs J; 1992; 10(2):22-5. PubMed ID: 1623438 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]