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Journal Abstract Search

328 related items for PubMed ID: 16696189

  • 1. Technical Report No. 38. Manufacturing chromatography systems postapproval changes (ChromPAC): chemistry, manufacturing, and controls documentation.
    PDA Manufacturing Chromatography Systems PAC Taskforce.
    PDA J Pharm Sci Technol; 2006 Mar; 60(1 Suppl TR38):1-29. PubMed ID: 16696189
    [No Abstract] [Full Text] [Related]

  • 2. 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; 104(3):803-12. PubMed ID: 25830179
    [Abstract] [Full Text] [Related]

  • 3. Top ten hot topics in parenteral science and technology.
    Akers MJ, Nail SL, Saffell-Clemmer W.
    PDA J Pharm Sci Technol; 2007 Mar; 61(5):337-61. PubMed ID: 18047174
    [Abstract] [Full Text] [Related]

  • 4. Equipment and analytical companies meeting continuous challenges. May 20-21, 2014 Continuous Manufacturing Symposium.
    Page T, Dubina H, Fillipi G, Guidat R, Patnaik S, Poechlauer P, Shering P, Guinn M, Mcdonnell P, Johnston C.
    J Pharm Sci; 2015 Mar; 104(3):821-31. PubMed ID: 25448273
    [Abstract] [Full Text] [Related]

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  • 6. Emerging technology: A key enabler for modernizing pharmaceutical manufacturing and advancing product quality.
    O'Connor TF, Yu LX, Lee SL.
    Int J Pharm; 2016 Jul 25; 509(1-2):492-498. PubMed ID: 27260134
    [Abstract] [Full Text] [Related]

  • 7. Current issues in validation of chromatography.
    Sofer G.
    Dev Biol (Basel); 2003 Jul 25; 113():61-4. PubMed ID: 14620853
    [Abstract] [Full Text] [Related]

  • 8. White paper on continuous bioprocessing. May 20-21, 2014 Continuous Manufacturing Symposium.
    Konstantinov KB, Cooney CL.
    J Pharm Sci; 2015 Mar 25; 104(3):813-20. PubMed ID: 25417595
    [Abstract] [Full Text] [Related]

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  • 10. Control systems engineering in continuous pharmaceutical manufacturing. May 20-21, 2014 Continuous Manufacturing Symposium.
    Myerson AS, Krumme M, Nasr M, Thomas H, Braatz RD.
    J Pharm Sci; 2015 Mar 25; 104(3):832-9. PubMed ID: 25546650
    [Abstract] [Full Text] [Related]

  • 11. Achieving continuous manufacturing. May 20-21, 2014 Continuous Manufacturing Symposium.
    Badman C, Trout BL.
    J Pharm Sci; 2015 Mar 25; 104(3):779-80. PubMed ID: 25501284
    [No Abstract] [Full Text] [Related]

  • 12. Achieving continuous manufacturing: technologies and approaches for synthesis, workup, and isolation of drug substance. May 20-21, 2014 Continuous Manufacturing Symposium.
    Baxendale IR, Braatz RD, Hodnett BK, Jensen KF, Johnson MD, Sharratt P, Sherlock JP, Florence AJ.
    J Pharm Sci; 2015 Mar 25; 104(3):781-91. PubMed ID: 25470351
    [Abstract] [Full Text] [Related]

  • 13. Opportunities and challenges of real-time release testing in biopharmaceutical manufacturing.
    Jiang M, Severson KA, Love JC, Madden H, Swann P, Zang L, Braatz RD.
    Biotechnol Bioeng; 2017 Nov 25; 114(11):2445-2456. PubMed ID: 28710854
    [Abstract] [Full Text] [Related]

  • 14. Quality Assurance and Quality Control, Part 2.
    Akers MJ.
    Int J Pharm Compd; 2015 Nov 25; 19(3):215-21. PubMed ID: 26714362
    [Abstract] [Full Text] [Related]

  • 15. Best practices for the development, scale-up, and post-approval change control of IR and MR dosage forms in the current quality-by-design paradigm.
    Van Buskirk GA, Asotra S, Balducci C, Basu P, DiDonato G, Dorantes A, Eickhoff WM, Ghosh T, González MA, Henry T, Howard M, Kamm J, Laurenz S, MacKenzie R, Mannion R, Noonan PK, Ocheltree T, Pai U, Poska RP, Putnam ML, Raghavan RR, Ruegger C, Sánchez E, Shah VP, Shao ZJ, Somma R, Tammara V, Thombre AG, Thompson B, Timko RJ, Upadrashta S, Vaithiyalingam S, Manufacturing Technical Committee of the Product Quality Research Institute.
    AAPS PharmSciTech; 2014 Jun 25; 15(3):665-93. PubMed ID: 24578237
    [Abstract] [Full Text] [Related]

  • 16. Emerging Technology as a Key Enabler for Modernizing Pharmaceutical Manufacturing.
    Lee SL, Brorson K.
    PDA J Pharm Sci Technol; 2017 Jun 25; 71(2):66-67. PubMed ID: 28396563
    [No Abstract] [Full Text] [Related]

  • 17. Dry-heat Depyrogenation Ovens for Pharmaceutical Compounding Facilities.
    Weller T, Kragseth R, Dullinger R, Illum H, Perry A.
    Int J Pharm Compd; 2015 Jun 25; 19(3):182-92. PubMed ID: 26714359
    [Abstract] [Full Text] [Related]

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  • 19. WHO Expert Committee on Specifications for Pharmaceutical Preparations.
    World Health Organization.
    World Health Organ Tech Rep Ser; 2011 Jun 25; (961):1-428, back cover. PubMed ID: 21699061
    [Abstract] [Full Text] [Related]

  • 20. Process analytical technology in the pharmaceutical industry: a toolkit for continuous improvement.
    Scott B, Wilcock A.
    PDA J Pharm Sci Technol; 2006 Jun 25; 60(1):17-53. PubMed ID: 17089677
    [Abstract] [Full Text] [Related]

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