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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

162 related items for PubMed ID: 19455941

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  • 2. Cleaning verification: A five parameter study of a Total Organic Carbon method development and validation for the cleaning assessment of residual detergents in manufacturing equipment.
    Li X, Ahmad IAH, Tam J, Wang Y, Dao G, Blasko A.
    J Pharm Biomed Anal; 2018 Feb 05; 149():33-39. PubMed ID: 29100028
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  • 3. Cleaning validation of ofloxacin on pharmaceutical manufacturing equipment and validation of desired HPLC method.
    Arayne MS, Sultana N, Sajid SS, Ali SS.
    PDA J Pharm Sci Technol; 2008 Feb 05; 62(5):353-61. PubMed ID: 19055231
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  • 6. In situ monitoring of soil dissolution dynamics: a rapid and simple method for determining worst-case soils for cleaning validation.
    Sharnez R, Lathia J, Kahlenberg D, Prabhu S, Dekleva M.
    PDA J Pharm Sci Technol; 2004 Feb 05; 58(4):203-14. PubMed ID: 15368990
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  • 8. Regulatory and quality considerations for continuous manufacturing. May 20-21, 2014 Continuous Manufacturing Symposium.
    Allison G, Cain YT, Cooney C, Garcia T, Bizjak TG, Holte O, Jagota N, Komas B, Korakianiti E, Kourti D, Madurawe R, Morefield E, Montgomery F, Nasr M, Randolph W, Robert JL, Rudd D, Zezza D.
    J Pharm Sci; 2015 Mar 05; 104(3):803-12. PubMed ID: 25830179
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  • 12. Cleaning Validation for Residual Estimation of Mometasone Furoate on Stainless-Steel Surface of Pharmaceutical Manufacturing Equipment Using a UHPLC-UV Method.
    Coelho AS, Arribada RG, Lages EB.
    PDA J Pharm Sci Technol; 2020 Mar 05; 74(1):41-48. PubMed ID: 31420502
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  • 13. Current issues in validation of chromatography.
    Sofer G.
    Dev Biol (Basel); 2003 Mar 05; 113():61-4. PubMed ID: 14620853
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  • 15. Comparative study of the swabbing properties of seven commercially available swab materials for cleaning verification.
    Corrigan DK, Piletsky S, McCrossen S.
    PDA J Pharm Sci Technol; 2009 Mar 05; 63(2):184-93. PubMed ID: 19634356
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  • 16. Risk management, cGMP, and the evolution of aseptic processing technology.
    Agalloco J, Akers J, Baseman H, Boeh R, Madsen R, Ostrove S, Pavell A.
    PDA J Pharm Sci Technol; 2009 Mar 05; 63(1):8-10. PubMed ID: 19455938
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  • 18. Determining the Clearance of Degraded Protein via a Monoclonal Antibody Purification Process in Support of Cleaning Carryover Limits in Multiproduct Facilities.
    Che PL, Bailey AP, Tam CYJ, Alvarez M, Arroyo AY.
    PDA J Pharm Sci Technol; 2020 Mar 05; 74(4):377-393. PubMed ID: 32179711
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