Analytical Method Development and Validation of Remdesivir in Bulk and Pharmaceutical Dosage Forms Using Reverse-Phase-High Performance Liquid Chromatography

Authors

  • K. Monika Raasi

DOI:

https://doi.org/10.22377/ijpscr.v1i2.35

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Published

2021-08-12

How to Cite

Raasi, K. M. . (2021). Analytical Method Development and Validation of Remdesivir in Bulk and Pharmaceutical Dosage Forms Using Reverse-Phase-High Performance Liquid Chromatography. B R Nahata Smriti Sansthan International Journal of Phramaceutical Sciences & Clinical Research, 1(2). https://doi.org/10.22377/ijpscr.v1i2.35

Issue

Vol. 1 No. 2 (2021): International Journal of Pharmaceutical Sciences and Clinical Research

Section

Original Article

License

This is an Open Access article distributed under the terms of the Attribution-Noncommercial 4.0 International License [CC BY-NC 4.0], which requires that reusers give credit to the creator. It allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, for noncommercial purposes only.