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4. 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]
6. Panel discussion: environmental sampling in an aseptic environment. I. Microbiological environmental monitoring. Raiman HL. Bull Parenter Drug Assoc; 1974; 28(6):253-60. PubMed ID: 4616742 [No Abstract] [Full Text] [Related]
7. [Studies on the microbial content in the air of pharmaceutical laboratories]. Wanner HU. Pharm Acta Helv; 1969 Sep; 44(9):517-34. PubMed ID: 4898236 [No Abstract] [Full Text] [Related]
8. [Bioengineering, pharmaceutical development and control of contamination: the three components of pharmaceutical engineering and their influence in advanced methods of production]. Ghirardini M, Falini R. Boll Chim Farm; 1986 Sep; 125(9):328-38. PubMed ID: 3828099 [No Abstract] [Full Text] [Related]