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Journal Abstract Search
119 related items for PubMed ID: 7165749
41. Determination and application of the permitted daily exposure (PDE) for topical ocular drugs in multipurpose manufacturing facilities. Lovsin Barle E, Bizec JC, Glogovac M, Gromek K, Winkler GC. Pharm Dev Technol; 2018 Mar; 23(3):225-230. PubMed ID: 28361586 [Abstract] [Full Text] [Related]
42. Overview of "The Study in Risk-Based Manufacturing Environmental Control for Non-Sterile Drug Products". Shirokizawa O, Inoue K, Kamikukita T. PDA J Pharm Sci Technol; 2021 Mar; 75(6):490-505. PubMed ID: 33990419 [Abstract] [Full Text] [Related]
43. Current practice in the operation and validation of aseptic blow-fill-seal processes. Ljungqvist B, Reinmüller B, Löfgren A, Dewhurst E. PDA J Pharm Sci Technol; 2006 Mar; 60(4):254-8. PubMed ID: 17089694 [Abstract] [Full Text] [Related]
47. The presence of drug in control samples during toxicokinetic investigations--a Novartis perspective. Nicholls I, Kolopp M, Pommier F, Scheiwiller M. Regul Toxicol Pharmacol; 2005 Jul; 42(2):172-8. PubMed ID: 15885865 [Abstract] [Full Text] [Related]
48. Contamination control in contract filling of small volume parenterals. Sherman NE. Bull Parenter Drug Assoc; 1970 Jul; 24(3):148-52. PubMed ID: 5422903 [No Abstract] [Full Text] [Related]
54. [Certification of suitability of monographs of the European pharmacopoeia]. Artiges A. Ann Pharm Fr; 2002 Sep; 60(5):333-40. PubMed ID: 12378143 [Abstract] [Full Text] [Related]