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2. Finding key impurities in different manufacturing routes of a drug substance using liquid chromatography/mass spectrometry followed by principal components analysis. Carrier D, Eckers C, Arnoult T, Thurston T, Major H. Rapid Commun Mass Spectrom; 2007; 21(23):3946-8. PubMed ID: 17975854 [No Abstract] [Full Text] [Related]
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6. Some problems associated with sterility testing in a commercial organization. Gasson AG. Dev Biol Stand; 1974 May 03; 23():151-6. PubMed ID: 4459189 [No Abstract] [Full Text] [Related]
9. [Problems of microbial contamination in pharmaceutical services (author's transl)]. Hilbig B, Schobess B, Vater U, Vater W, Walker R. Pharmazie; 1981 Apr 03; 36(2):147-54. PubMed ID: 7232486 [Abstract] [Full Text] [Related]
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11. Validation and environmental monitoring of aseptic processing. Committee on Microbial Purity. J Parenter Sci Technol; 1990 Apr 03; 44(5):272-7. PubMed ID: 2250203 [Abstract] [Full Text] [Related]
19. [Validation of procedure for sterile manufacturing. Simulated distribution in containers, in a sterile area]. Arecco D, Carazzone M, Fava M. Boll Chim Farm; 1982 Oct 03; 121(10):493-502. PubMed ID: 7165749 [No Abstract] [Full Text] [Related]