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7. Aseptic process monitoring--a better strategy. Validation Group, Inc. Wilson JD PDA J Pharm Sci Technol; 1999; 53(3):111-4. PubMed ID: 10754699 [No Abstract] [Full Text] [Related]
8. PDA comments: PIC draft recommendations on the inspection of isolator technology. Parenteral Drug Association. PDA J Pharm Sci Technol; 1999; 53(3):141-7. PubMed ID: 10754704 [No Abstract] [Full Text] [Related]
9. [Validation of sterile pharmaceutical production. Considerations and experiences]. Pongiluppi S Boll Chim Farm; 1985 Jul; 124(7):293-305. PubMed ID: 4074520 [No Abstract] [Full Text] [Related]
10. [Education and training of personnel in the clean rooms. Examination from the viewpoint of the microbiologist]. Zuger A Swiss Dent; 1983; 4(1-2):27-8, 29-30, 33-5. PubMed ID: 6408766 [No Abstract] [Full Text] [Related]
11. Rapid/automated ID methods survey. PDA Microbial ID Task Force. Parenteral Drug Association. J Parenter Sci Technol; 1990; 44(4):216-22. PubMed ID: 2213430 [No Abstract] [Full Text] [Related]
13. Sterility testing of ophthalmic ointments using isopropyl myristate. Robertson JH Bull Parenter Drug Assoc; 1974; 28(6):288-94. PubMed ID: 4455325 [No Abstract] [Full Text] [Related]
14. 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]