Parul Institute of Pharmacy

Dr. Falguni Tandel

falguni-tandel
Designation : Professor & HOD
Total Exp : 14.6 Years
Educational Qualification : M.Pharm., PhD
Research Area :
Analytical method development and validation for assay method, stability indicating method, bioanalytical method with pharmacokinetic study with Quality by Design approach, formulation development with risk assessment studies and Polyherbal formulation development and evaluation

Dr. Falguni Tandel is currently working as Professor & HOD of QA department, in Parul Institute of Pharmacy. She has 14.6 years of academic and industrial experience. She have actively contributed in field of research for last ten years. She is guiding 4 PhD students. She guided 37 M.Pharm students and 2 are currently under guidance. She is Co-Guide of 3 MD students of Ayurveda too.
She has 21 national as well as international papers published to my credit. She presented 20 oral/posters in national as well as international conferences.
Her research interest includes analytical method development and validation for assay method, stability indicating method, bioanalytical method with pharmacokinetic study with Quality by Design approach, formulation development with risk assessment studies and Polyherbal formulation development and evaluation.
She is skilled in handling and validating HPLC with troubleshooting. Instrumental expertise includes HPLC, UV, FTIR, Spectro fluorophotometer, Polarimeter, Karlfischer, Autotitrator etc.
She have 2 years industrial experience in QA and QC department of the injectable manufacturing plant where I had experience of testing of Raw Material, Stability Study sample, Finished product, Water, ETP as other materials. I am skilled in QA documents preparation specially SOPs, Specifications, Validation protocol, Validation report and Standard Testing Procedures.

Contact Information
Office Phone02668-260232
Email[email protected]
Membership
APTI , IPA, ACS(American Chemical Society)
Specialization
Specialization AreasPharmaceutical Quality Assurance, Spectroscopy, Chromatography and other separation techniques, Method Development and Validation with AQbD approach, GMP, Regulatory Affairs, Drug Approval Process, V alidation of Instruments, Document Preparation

International/National Journal Papers

[1] Sadhana J.Rajput, Falguni T. Patel, Study of Lipophilicity Profile of Mosapride Citrate Dihydrate, Indian journal of pharmaceutical sciences, Vol-67, 508-510,2005.

[2] S.J.Rajput, M.G.Sankalia, F.T.Patel, Spectrofluorophotometric determination of rofecoxib and mosapride citrate in their individual dosage form, Indian journal of pharmaceutical sciences, Vol-67, 582-585, 2005.

[3] Falguni Tandel, Rajesh K.S., Charulben Nakarani, Nidhi Patel, Kinjal Shah, Priyanka Patel, S.S.Pandya, Simple and derivative UV spectroscopic method for the estimation of anti- inflammatory agent, Pharma science monitor, Vol-67,2131-2138, 2012.

[4] Falguni Tandel, Rajesh K.S., Nikita Patel, Khurshid Molvi, S.S.Pandya, Estimation of anti- inflammatory agent by derivative and simple UV spectroscopic methods, World journal of pharmacy and pharmaceutical sciences, Vol-1,1064-1072, 2012.

[5] Patel Nisha, Tandel Falguni, Shah Swati, Patel Mohit, Patel Amit, Method Development and Validation for the Simultaneous Estimation of Meropenem and Sulbactam Sodium, Current Pharma Research, Volume-2, 480-486 , 2012.

[6] Nikita N. Patel, Parag R. Patel, Falguni A. Tandel, Charmy S. Kothari, Shailesh A. Shah Ratio derivative spectrophotometric method for simultaneous estimation of olmesartan medoxomil and atorvastatin calcium in their combined tablet dosage form, International Journal of Pharmacy & Pharmaceutical Sciences, Volume-4,222-226, 2012.

[7] Nikita N. Patel, Parag R. Patel, Falguni A. Tandel, Karuna J. Patel, Ujjaval N. Limbachiya, Charmy S. Kothari, Quality Audit: Regulatory Compliance in Pharmaceuticals, World journal of pharmacy and pharmaceutical sciences, Vol-1,1064-1072,2012.

[8] Megha Pancholi, Falguni Tandel, Nikita Patel, Absorption ratio method for simultaneous estimation of dicyclomine hydrochloride and dexketoprofen trometamol, Asian journal of research in chemistry,Vol-6, Issue-12, 1169-1172, 2013.

[9] Bhagavati Solanki, Harshal Trivedi, Ankita Khodiyar, Falguni Tande1, Lalit Lata Jha, Development And Validation of Derivative Spectroscopic Method For Estimation of Acebrophylline In Bulk And Its Dosage Form & In Presence of Impurity, Ambroxol HCl, PHARMAGENE , Vol:1 Issue:1 ; 7-11, 2013.

[10] Tandel Falguni, Shah Swati , Patel Hiren, Patel Nikita, Rajesh KS, Development and Validation of Ratio Derivative Spectrophotometric Method for Determination of Aliskiren Hemifumarate and Valsartan, PHARMAGENE, Vol:1 Issue:2; 49-53, 2013.

[11] Shreyasi Chaudhuri, Falguni Tandel, Kinesh Patel, J J Chaudhuri, RP-HPLC Method for Simultaneous Estimation of Rabeprazole Sodium and Domperidone in Soft Gelatin Capsule, Inventi Rapid: Pharm Analysis & Quality Assurance, Issue 3, Vol. 2014.

[12] Nidhi S. Patel, Falguni B. Tandel, Yogita D. Patel, Kartavya B. Thakkar, Development and Validation of Stability indicating HPLC Method for Simultaneous Estimation of Cefixime and Linezolid, Indian journal of pharmaceutical sciences,Vol-76, 535-540, 2014.

[13] Nikita Patel, Pinal Rathwa, Falguni Tandel, Parag Patel, Binal Mistry, Development anad validation of first order derivative spectrophotometric mehod for estimation of Azilsartan kamedoxomil and Chlorthalidone in combined tablet dosage form, PHARMAGENE, Vol:2 Issue:4; 19-23, 2015.

[14] Dukandar AD, Tandel FB, Jha LL, Prajapati M, Process Validation of Ibuprofen Film Coated Tablets, International Journal for Pharmaceutical Research Scholars (IJPRS),Vol- 4, issue – 2,169-188, 2015.

[15] Anand B. Pithadia, Dineshkumar, M. Prajapati, Lalit Lata Jha, Falguni Tandel, Nikita Patel, Bioanalytical Method Development And Validation Of Hcg (Human Chorionic Gonadotropin), International Journal of Pharmacy and Pharmaceutical Sciences , Vol 7, Issue 7, 390-396, 2015.

[16] Falguni B.Tandel, Hardik G.Prajapati, Nikita Patel, Kinjsl Parmar, Simultaneous estimation of Eperisone Hydrochloride and Diclofenac Sodium in bulk and capsule dosage form by absorption correction method, PHARMAGENE, Vol:2 Issue:4; 15-18, 2015.

[17] Kinjal A. Parmar, Falguni B. Tandel, Dinesh Rabari, Analytical Method Development and Validation of Desloratadine Tablet, Research Journal of Pharmacy and Technology,Vol: 8, Issue: 6;693-696, 2015.

[18] Jainul Bhayji, Falguni Tandel, Nikita Patel, Analytical Method Development and Validation for Simultaneous Estimation of Bromocriptine Mesylate and Metformin Hydrochloride with DOE Approach, World journal of pharmacy and pharmaceutical sciences, Vol-4, Issue: 8, 656-665, 2015.

[19] Riddhi Parmar, Falguni Tandel, Nikita Patel, Ratio spectra derivative UV spectrophotometric method for simultaneous estimation of Ketorolac tromethamine and Phenylephrine hydrochloride in immediate release tablet, International Journal of Pharmacy and Pharmaceutical Sciences , Vol 7, Issue 11, 13-16, 2015.

[20] Shah Krutika, Tandel Falguni, Lalcheta Sagar, A Sensitive Spectrophotometric Method For Simultaneous Estimation Of Prasugrel Hydrochloride And Aspirin , PHARMAGENE, Vol:3 Issue:3; 1-5, 2015.

[21] Ghanshyam G Solanki, Lalit Lata Jha, Falguni B Tandel, Lalcheta Sagar, Simultaneous Estimation of Mefenamic Acid and Tizanidine in Tablet Dosage Form by Dual Wavelength Method, Inventi Rapid: Pharm Analysis & Quality Assurance, Vol. 2017Issue 1, 1-4, 2017.

International/National Conference Papers

[1] Spectrofluorophotometric Estimation of Mosapride Citrate Dihydrate in Bulk Drug and in its Marketed Formulation, 54th Indian Pharmaceutical Congress, Oral, 14th December, 2002.

[2] First Order Derivative Spectroscopic for simultaneous estimation of Cefixime trihydrate and Levofloxacin hemihydrate in combined tablet Dosage form, Sumandeep Vidyapeeth, Poster, 22-23 February, 2013.

[3] Use of Response Surface Methodology for development of New first order derivative spectrophotometric method for simultaneous determination of Montelukast sodium and Olopatadin hydrochloride in bulk, GTU , Supported by De Montfort University, Leicester, Poster, 16-17 March, 2013.

[4] First Order Derivative Spectroscopic Method and Rp-Hplc Method of estimation of Cefixime trihydrate and Levofloxacin hemihydrate in Dosage form, Sigma Institute of Pharmacy, Poster, 17-18 August, 2013.

[5] Development and validation of stability indicating HPLC method for simultaneous estimation of cefixime and linezolid, Sigma Institute of Pharmacy, Poster, 17-18 August, 2013.

[6] Kinetic degradation study and stability indicating method for related substances and assay of tazobactum sodium and pipericillin sodium, 66th Indian Pharmaceutical Congress, Oral, 14th December, 2015.

[7] Development and Validation of Assay method and Stability Indicating Method of Tolperison HCl and Diclofenac Sodium, Parul Institute of Pharmacy, Poster, January, 30-31, 2017.

[8] Isomeric Separation of Xylidine and its estimation in Pharmaceutical Dosage Form, Parul Institute of Pharmacy, Poster, January, 30-31, 2017.

[9] Optimization and screening of nanoparticle loaded topical gel of Deflazacort, Sumandeep Vidyapeeth, Poster, March, 17-18, 2017.

[10] Formulation development for Ketorolac tromethamine and Phenylephrine HCl immediate release tablet using 32 full factorial design, Sumandeep Vidyapeeth, Poster, March, 17-18, 2017.

[11] Development and validation of UV spectrophotometric method for simultaneous estimation of Montelukast sodium and Olopatadine HCl using DoE approach, Sumandeep Vidyapeeth, Poster, March, 17-18,2017.

[12] DoE approach for RP-HPLC method development and validation for simultaneous estimation of Bromocriptine mesylate and Metformin HCl, Sumandeep Vidyapeeth, Poster, March, 17-18, 2017.

[13] Simple and Derivative UV Spectrophotometric method for the estimation of anti- inflammatory agent, Nirma Uni., institute of Pharmacy, Poster, 12-13 November, 2011.

[14] RP-HPLC Method for the estimation of Anti-Inflammatory Agent, Nirma Uni., institute of Pharmacy, Poster, 12-13 November , 2011.

[15] RPHPLC- PDA stability indicating method for simultaneous estimation of paracetamol and pamabrome, Parul University, Faculty of Pharmacy, Poster, March 4-5,2016.

[16] Nanotechnology for topical gel preparation of Deflazacort, Parul University, Faculty of Pharmacy, Poster, March 4-5, 2016.

[17] Estimation of entrapment efficiency of carvacol loaded nanobeads, Parul University, Faculty of Pharmacy, Poster, 7/4/17 & 8/4/17.

[18] Estimatiion of related substances of budosanide by HPLC, Parul University, Faculty of Pharmacy, Poster, 7/4/17 & 8/4/17.

[19] Stability indicating method development and validation for benzocaine and diclifenac sodium gel, Parul University, Faculty of Pharmacy, Oral, 7/4/17 & 8/4/17.

Fund Type Agency Start Date Duration Investigators
Research Grant GUJCOST/MRP 28th March 2016 2 Years Dr. Sulekha Bhadra, Dr. Falguni Tandel

Patents Filed

[1] I have filed a patent on “Metformin and Bromocriptine formulation with Different Release Profile”. With Shivpal Sarvaiya. Application Number of patent is 201721014738 and Date is 26/04/2017.