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Page 1
A Quantitative Study of US FDA Inspection Data for Drug Manufacturing Sites.
Ther Innov Regul Sci. 2020 Jul;54(4):725-730. doi: 10.1007/s43441-019-00015-3. Epub 2019 Dec 4.
Ther Innov Regul Sci. 2020.
PMID: 32557291
Review.
A Semiquantitative Risk Assessment Methodology Fit for Biopharmaceutical Life Cycle Stages.
Pazhayattil AB, Sayeed-Desta N, Chen S, Ingram M.
Pazhayattil AB, et al.
PDA J Pharm Sci Technol. 2020 Jul-Aug;74(4):423-434. doi: 10.5731/pdajpst.2019.010173. Epub 2020 Feb 14.
PDA J Pharm Sci Technol. 2020.
PMID: 32060222
Review.
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Assessment Methodology for Process Validation Lifecycle Stage 3A.
Sayeed-Desta N, Pazhayattil AB, Collins J, Chen S, Ingram M, Spes J.
Sayeed-Desta N, et al. Among authors: pazhayattil ab.
AAPS PharmSciTech. 2017 Jul;18(5):1881-1886. doi: 10.1208/s12249-016-0641-9. Epub 2016 Oct 6.
AAPS PharmSciTech. 2017.
PMID: 27714700
Review.
Item in Clipboard
A Science and Risk-Based Pragmatic Methodology for Blend and Content Uniformity Assessment.
Sayeed-Desta N, Pazhayattil AB, Collins J, Doshi C.
Sayeed-Desta N, et al. Among authors: pazhayattil ab.
AAPS PharmSciTech. 2018 Apr;19(3):1483-1492. doi: 10.1208/s12249-017-0925-8. Epub 2017 Dec 6.
AAPS PharmSciTech. 2018.
PMID: 29214608
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The value of AI based CT severity scoring system in triage of patients with Covid-19 pneumonia as regards oxygen requirement and place of admission.
Kohli A, Jha T, Pazhayattil AB.
Kohli A, et al. Among authors: pazhayattil ab.
Indian J Radiol Imaging. 2021 Jan;31(Suppl 1):S61-S69. doi: 10.4103/ijri.IJRI_965_20. Epub 2021 Jan 23.
Indian J Radiol Imaging. 2021.
PMID: 33814763
Free PMC article.
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