These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

386 related articles for article (PubMed ID: 34205797)

  • 1. Process Analytical Technology Tools for Monitoring Pharmaceutical Unit Operations: A Control Strategy for Continuous Process Verification.
    Kim EJ; Kim JH; Kim MS; Jeong SH; Choi DH
    Pharmaceutics; 2021 Jun; 13(6):. PubMed ID: 34205797
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Toward Higher QA: From Parametric Release of Sterile Parenteral Products to PAT for Other Pharmaceutical Dosage Forms.
    Hock SC; Constance NX; Wah CL
    PDA J Pharm Sci Technol; 2012; 66(4):371-91. PubMed ID: 22767885
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chemometrics-based process analytical technology (PAT) tools: applications and adaptation in pharmaceutical and biopharmaceutical industries.
    Challa S; Potumarthi R
    Appl Biochem Biotechnol; 2013 Jan; 169(1):66-76. PubMed ID: 23138336
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Process Analytical Technology for Crystallization of Active Pharmaceutical Ingredients.
    Malwade CR; Qu H
    Curr Pharm Des; 2018; 24(21):2456-2472. PubMed ID: 29956616
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Process analytical technology (PAT) for biopharmaceutical products.
    Rathore AS; Bhambure R; Ghare V
    Anal Bioanal Chem; 2010 Sep; 398(1):137-54. PubMed ID: 20480150
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The development and validation of a quality by design based process analytical tool for the inline quantification of Ramipril during hot-melt extrusion.
    Dadou SM; Senta-Loys Z; Almajaan A; Li S; Jones DS; Healy AM; Tian Y; Andrews GP
    Int J Pharm; 2020 Jun; 584():119382. PubMed ID: 32360547
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Methodology and application of process analytical technology (PAT) for traditional Chinese medicine manufacturing:a review].
    Xiong HS; Zhang Q; Zhang SN; Cai JY; Su J; Zhu YH; Yan KJ
    Zhongguo Zhong Yao Za Zhi; 2023 Jan; 48(1):22-29. PubMed ID: 36725254
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Understanding pharmaceutical quality by design.
    Yu LX; Amidon G; Khan MA; Hoag SW; Polli J; Raju GK; Woodcock J
    AAPS J; 2014 Jul; 16(4):771-83. PubMed ID: 24854893
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Application of process analysis technology in traditional Chinese medicine manufacturing industry].
    Zhu WF; Shen Y; Deng P; Fei YC; Xiao ZQ; Zhong ZJ
    Zhongguo Zhong Yao Za Zhi; 2024 May; 49(9):2299-2307. PubMed ID: 38812130
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Application of Process Analytical Technology for Pharmaceutical Coating: Challenges, Pitfalls, and Trends.
    Feng H; Mohan S
    AAPS PharmSciTech; 2020 Jun; 21(5):179. PubMed ID: 32596747
    [TBL] [Abstract][Full Text] [Related]  

  • 11. PAT implementation for advanced process control in solid dosage manufacturing - A practical guide.
    Sacher S; Poms J; Rehrl J; Khinast JG
    Int J Pharm; 2022 Feb; 613():121408. PubMed ID: 34952147
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Implementation of an advanced hybrid MPC-PID control system using PAT tools into a direct compaction continuous pharmaceutical tablet manufacturing pilot plant.
    Singh R; Sahay A; Karry KM; Muzzio F; Ierapetritou M; Ramachandran R
    Int J Pharm; 2014 Oct; 473(1-2):38-54. PubMed ID: 24974987
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Advances in Twin-Screw Granulation Processing.
    Nandi U; Trivedi V; Ross SA; Douroumis D
    Pharmaceutics; 2021 Apr; 13(5):. PubMed ID: 33925577
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Product Development, Manufacturing, and Packaging of Solid Dosage Forms Under QbD and PAT Paradigm: DOE Case Studies for Industrial Applications.
    Singh BN
    AAPS PharmSciTech; 2019 Sep; 20(8):313. PubMed ID: 31529232
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Application of quality by design in the current drug development.
    Zhang L; Mao S
    Asian J Pharm Sci; 2017 Jan; 12(1):1-8. PubMed ID: 32104308
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 114(11):2445-2456. PubMed ID: 28710854
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Can Continuous Manufacturing of Topical Semisolids by Hot Melt Extrusion Soon Be a Reality?
    Matadh AV; Echanur A; Suresh S; Chede L; Maibach H; Kulkarni V; Murthy SN; H N S
    Mol Pharm; 2023 Aug; 20(8):3779-3790. PubMed ID: 37421361
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multivariate analysis in the pharmaceutical industry: enabling process understanding and improvement in the PAT and QbD era.
    Ferreira AP; Tobyn M
    Pharm Dev Technol; 2015; 20(5):513-27. PubMed ID: 24641280
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Supervisory control system for monitoring a pharmaceutical hot melt extrusion process.
    Markl D; Wahl PR; Menezes JC; Koller DM; Kavsek B; Francois K; Roblegg E; Khinast JG
    AAPS PharmSciTech; 2013 Sep; 14(3):1034-44. PubMed ID: 23797304
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The physical stability of drugs linked to quality-by-design (QbD) and in-process technology (PAT) perspectives.
    Aucamp M; Milne M
    Eur J Pharm Sci; 2019 Nov; 139():105057. PubMed ID: 31470099
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.