Author(s): Anali Sawant, Seema Kamath, Hemanth Katta G, Muddukrishna Badamane Sathyanarayana, Ravindra Shenoy, Girish Pai K

Email(s): girish.pai@manipal.edu

DOI: 10.52711/0974-360X.2022.00121

Address: Anali Sawant1, Seema Kamath1, Hemanth Katta G1, Muddukrishna Badamane Sathyanarayana2, Ravindra Shenoy3, Girish Pai K1*
1Department of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Udupi, Karnataka, 576104, India.
2Department of Pharmaceutical Quality Assurance, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Udupi, Karnataka, 576104, India.
3Department of Commerce, Manipal Academy of Higher Education, Manipal, Udupi, Karnataka, 576104, India.
*Corresponding Author

Published In:   Volume - 15,      Issue - 2,     Year - 2022


Cite this article:
Anali Sawant, Seema Kamath, Hemanth Katta G, Muddukrishna Badamane Sathyanarayana, Ravindra Shenoy, Girish Pai K. Investigation of manufacturing defects and cGMP lessons learnt from quality issues in Pharmaceutical Sterile Preparations. Research Journal of Pharmacy and Technology. 2022; 15(2):729-5. doi: 10.52711/0974-360X.2022.00121




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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

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