Quantitative structure retention relationship (QSRR) approach for assessment of chromatographic behavior of antiviral drugs in the development of liquid chromatographic method

Author:

Paritala Jagadeesh1ORCID,Peraman Ramalingam2ORCID,Kondreddy Vinod Kumar1,Subrahmanyam C. V. S.3,Ravichandiran V24

Affiliation:

1. Department of Pharmaceutical Analysis, Raghavendra Institute of Pharmaceutical Education and Research (RIPER)-Autonomous, Anantapur, India

2. Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education and Research (NIPER), Hajipur, Bihar, India

3. Gokaraju Rangaraju College of Pharmacy, Osmania University, Hyderabad, India

4. National Institute of Pharmaceutical Education & Research (NIPER), Kolkata, India

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Reference34 articles.

1. ICH Harmonized Guideline Q12. Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management, 2017.

2. Food Drug Administration. Pharmaceutical Quality System (ICH 10) conference. Arlington, VA, 2011.

3. Analytical Quality by Design: A Tool for Regulatory Flexibility and Robust Analytics

4. Application of artificial neural networks in HPLC method development

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