Monitoring of Process Impurities in Drugs-Reference-Cited by-同舟云学术

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Monitoring of Process Impurities in Drugs

Published:1998 Issue: Volume: Page:833-888
ISSN:0301-4770
Container-title:Journal of Chromatography Library
language:
Short-container-title:

Author:

HUSAIN Sajid,RAO R. Nageswara

Publisher

Elsevier

Reference180 articles.

1. Quantitative Analysis Using Chromatographic Techniques;Jensen,1987

2. The FDA perspective on the development of stereoisomers

3. Creative Troubleshooting in the Chemical Process Industries;Saletan,1996

4. Therapeutic Drug Monitoring by Liquid Chromatography;Pippenger,1985

5. Text Book of Biopharmaceutic Analysis: A Description of Methods for the Determination of Drugs in Biologic Fluids;Smith,1981

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enantioselective recognition, synthesis, and separation of pharmaceutical compounds at chiral metallic surfaces;ChemMedChem;2024-02-02

2. Identification, Characterization, and the Determination of Process-related Impurities in Minodronic Acid Bulk Drug;Current Pharmaceutical Analysis;2022-03

3. Large scale purification and characterization of A21 deamidated variant-most prominent post translational modification (PTM) for insulins which is also widely observed in insulins pharmaceutical manufacturing and storage;Protein Expression and Purification;2021-09

4. Impurities in Drug Products and Active Pharmaceutical Ingredients;Critical Reviews in Analytical Chemistry;2016-11-01

5. Identification, characterization and HPLC quantification of process-related impurities in Trelagliptin succinate bulk drug: Six identified as new compounds;Journal of Pharmaceutical and Biomedical Analysis;2016-09

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