Mr. Prashant K. Chaturvedi
Qualification | B. Pharm., M. Pharm, Pursuing Ph.D. |
Designation | Assistant Professor |
Specialization | Pharmaceutical Chemistry |
Academic Experience | 11 Years St. John Institute of Pharmacy and Research, Palghar (2023 til date) |
Research Experience | Junior Research Fellowship (AICTE) (2006-2008) |
Industry Experience | 3 Years (2008 – 2011) Sandoz Pvt. Ltd. (a Novartis group company) Job Profile: Scientist analytical development (analytical method development and validation, characterization of impurities and technology transfer) |
Areas of Interest | Analytical method development and impurity profiling, Quality by design approach in analytical sciences. |
Subjects Taught | · Pharmaceutical Analysis · Modern Pharmaceutical Analytical Techniques · Audits and Regulatory Compliance · Organic Chemistry |
Presentations | International: – Nil National: – 04 |
1. Chaturvedi P.K., Joshi K., Tauro S.J., Chopra S., “Quality by Design based development of liquid chromatography method for separation of impurities of antiviral drug and characterization of these impurities by Tandem Mass spectrometry.” Indian Pharmacopoeia Commission & APTI sponsored international conference on “Current Scenario in Advancements of Pharmaceutical Education & Research: Challenges & Prospects” organized by Swami Vivekanand College of Pharmacy, Banur, Punjab from 29th – 31st December 2020. 2. Prashant Chaturvedi, Shruti Chopra, Savita Tauro, “Quality by design-based optimization of forced degradation and development of a stability indicating LC-MS compatible RP-HPLC assay method for the determination of Daclatasvir dihydrochloride” AICTE Sponsored National Conference on “QbD & PAT – An Essential Tool of Product Life Cycle Management”, SVKM’S Dr. Bhanuben Nanavati Colllege of Pharmacy, Mumbai, 28th-29th August 2019 3. Prashant Chaturvedi, “Optimization of forced degradation by factorial design and development of Liquid Chromatographic method for antiviral drug” Minor research project presentation (2017-18), University of Mumbai, Fort campus, 12th March, 2019 4. Prashant chaturvedi, Jineetkumar Gawad, Savita Tauro, “A developed and validated stability-indicating rp-hplc method for determination of felbinac in the presence of its degradation products as per international conference on harmonization guidelines” Savitribai Phule Pune University Sponsored Three Days National Level Seminar on “Structural Elucidation of Bioactive Compounds” Sinhgad Institute of Pharmaceutical Science, Lonavala, 5th -9th December, 2014 |
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Publications | International – 3 National – 0 |
1. Chaturvedi P., Gawad J., Tauro S., A validated stability indicating reverse phase -high performance liquid chromatographic method for determination of Felbinac, International Journal of Biological & Pharmaceutical Research, 2015; 6 (3): 205-210.
2. Chaturvedi P., Sharma R., Simultaneous Spectrophotomtric estimation and validation of Three Component Tablet Formulation Containing Metformin HCL, Pioglitazone HCL and Glibenclamide, Analytical Letters, Taylor and Francis, Canada. 41:2133-2142,2008 3. Chaturvedi P., Sharma R., Development and Validation of an RP-HPLC Method for simultaneous analysis of a Three-Component Tablet Formulation Containing Metformin HCL, Pioglitazone HCL and Glibenclamide, Acta Chrometographica, Poland 20(2008)3, 451-461 |
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Research Grants | 1. University of Mumbai, A. Y. 2017-18, for “Optimization of forced degradation by factorial design and development of Liquid Chromatographic method for antiviral drug”
2. University of Mumbai, A. Y. 2013-14, for “Development and validation of RP-HPLC method for stability indicating assay” |
Professional Memberships | · Regd. Pharmacist, No. 37185 · Indian Pharmaceutical Association (Life Member) · Indian Society for Technical Education (Life Member) |