Author(s):
Mansi H. Patel, Divya M. Jadav, Mitali Dalwadi, Ritika Gajre, Chainesh Shah, U. M. Upadhyay
Email(s):
patelmansi052001@gmail.com
DOI:
10.52711/0975-4377.2021.00053
Address:
Mansi H. Patel1*, Divya M. Jadav2, Mitali Dalwadi3, Ritika gajre4, Chainesh shah4, U. M. Upadhyay6
Department of Quality Assurance, Sigma Institute of Pharmacy, At., Post Bakrol, Ta: Waghodia, Dist: Vadodara-390019, Gujarat, India.
*Corresponding Author
Published In:
Volume - 13,
Issue - 4,
Year - 2021
ABSTRACT:
Impurities in medicine formulation aren't acceptable. It's defined as any undesired compounds or organic material found in Active Pharmaceutical Ingredients (APIs). Impurity are some things that's impure or makes something else impure. Even in minute amounts, the presence of those undesirable compounds might affect the efficacy and safety of medicinal medicines. Impurities don't always need to be inferior.
Cite this article:
Mansi H. Patel, Divya M. Jadav, Mitali Dalwadi, Ritika Gajre, Chainesh Shah, U. M. Upadhyay. Development of “Impurities Profiling” by using Morden Analytical Techniques: A Review. Research Journal of Pharmaceutical Dosage Forms and Technology. 2021; 13(4):329-4. doi: 10.52711/0975-4377.2021.00053
Cite(Electronic):
Mansi H. Patel, Divya M. Jadav, Mitali Dalwadi, Ritika Gajre, Chainesh Shah, U. M. Upadhyay. Development of “Impurities Profiling” by using Morden Analytical Techniques: A Review. Research Journal of Pharmaceutical Dosage Forms and Technology. 2021; 13(4):329-4. doi: 10.52711/0975-4377.2021.00053 Available on: https://rjpdft.com/AbstractView.aspx?PID=2021-13-4-10
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