Ramreddy Godela

Ramreddy Godela

Assistant Professor

Department of Pharmaceutical Analysis

GITAM School of Pharmacy

Hyderabad

Education

M. Pharm.

Ram Reddy Godela hails from Warangal, Telangana. He holds a PhD from GITAM (Deemed to be University) in Visakhapatnam. During his master's degree, he was a GPAT fellow, showcasing his dedication to advancing in pharmacy. His research interests lie in analytical method development and validation by HPLC, UV, and LC-MS. Additionally, he engages in interdisciplinary research within pharmaceutical science, mainly focusing on phytochemical investigations and pharmacological studies.

Research Publications

  • Godela R. An effective stability indicating RP-HPLC method for simultaneous estimation of Dolutegravir and Lamivudine in bulk and their tablet dosage form. Future Journal of Pharmaceutical Sciences. 2020 Dec;6:1-9. IF-2.6
  • Godela R, Gummadi S, Pathak S, Pola KK, Yagnambhatla R. RP-HPLC–PDA Approach for Concurrent Analysis of Telmisartan and Azelnidipine in Bulk and Commercial Tablets. Chemistry Africa. 2023 Feb;6(1):393-403. IF- 2.6
  • Pathak S, Godela R. Nardostachys jatamansi: Phytochemistry, ethnomedicinal uses, and pharmacological activities: A comprehensive review. Fitoterapia. 2023 Nov 30:105764. IF- 3.4
  • Pottekanti K, Godela R. Concurrent estimation of Pregabalin and Etoricoxib by new stability indicating RP-UPLC approach: application in assay of commercial tablets.Discover Applied Sciences. 2024 Nov; 6: 626. IF-2.8
  • Ponnekanti K, Godela R, Solipeta DR, Sujatha K, Beda DP. A novel RP-HPLC stability-indicating method for simultaneous estimation of Niraparib and Abiraterone in synthetic mixtures and combined tablet formulations. Discover Applied Sciences. 2025 May 17(5).

Ongoing Research Projects

  • Check Icon Characterization of degradation products of Voclosporin using liquid chromatography, mass spectrometry under forced degradation conditions (GITAM Research Seed Grant)

Expertise

  • Check Icon Analytical and Bio analytical method developments, Stability indicating HPLC and LC-MS methods, Impurity profiling, Characterization of degradation products and Phytochemicals, In-vitro Pharmacological studies
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