Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shahnawaz Sajid"'
Autor:
Ganesan, Thipashini a, b, Muthudoss, Prakash c, Voguri, Raja Sekhar d, Ghosal, Subhas e, Ann, Eddy Yii Chung c, Kwok, Jayson c, Shahnawaz, Sajid Syed a, Omar, Muhammad Firdaus f, Allada, Ravikiran a, g, ⁎⁎, See, Hong Heng b, g, ⁎
Publikováno v:
In Journal of Pharmaceutical Sciences December 2022 111(12):3318-3326
Akademický článek
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Publikováno v:
Recent advances in drug delivery and formulation. 15(1)
Co-crystal is an attractive alternative and a new class of solid forms because that can be engineered to have desired physicochemical properties. Co-crystals have gained considerable attention from the generic pharmaceutical industry after the USFDA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfbc250ff57858b4225b7a7b522fa74d
https://pubmed.ncbi.nlm.nih.gov/34602030
https://pubmed.ncbi.nlm.nih.gov/34602030
Autor:
Chandra Kant Belwal, Ramesh Kumar, Shahnawaz Sajid, Pawan Kumar, Muhammad Taufiq F. Mazlee, Muhammad K. Abdul Wahab
Publikováno v:
Chemical Papers. 73:39-46
An improved three-step process for the synthesis of gefitinib from readily available starting material is discussed in this protocol. The protocol is based on the synthesis, isolation, characterization of novel intermediates and their application in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb98227b9f175fa326d40748e7fc3127
https://doi.org/10.1007/s11696-018-0564-x
https://doi.org/10.1007/s11696-018-0564-x
Publikováno v:
PDA journal of pharmaceutical science and technology. 62(5)
Inadequate cleaning of a pharmaceutical manufacturing plant or inadequate purging of the individual pieces of equipment used in multi-product manufacturing or equipment not dedicated to individual products may lead to contamination of the next batch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0a888ccffa26ccda0596213620c7bfab
https://pubmed.ncbi.nlm.nih.gov/19055231
https://pubmed.ncbi.nlm.nih.gov/19055231
Publikováno v:
Analytical Methods. 2:397
The systematic approach developed to assess the amount of residues left on manufacturing equipment surfaces from product carryover is known as cleaning validation. Current trends have seen increasing demand for rapid sample analysis time along with l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b89d2ffd155ce67e2ecefab27996ad2
https://doi.org/10.1039/b9ay00278b
https://doi.org/10.1039/b9ay00278b