RC
RAMANKUMAR CHANDAK
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About
13 Years of Approved Teaching, Administrative, Experience in Pharmacy College. University (Dr. BAMU, Aurangabad) Department Of Pharmacognosy UG-Approved experience . Approved PG -Teacher in Pharmacy & Research guide in Quality Assurance , Chairman Nominee for Selection Committee as a Subject Expert for Approval process under Dr.BAMU, Aurangabad. Working as Joint Chief Supretendant under Exam. Board of Studies Dr. BAMU, Aurangabad. Member of Syllabus framing committee by Dr.Babasaheb Ambedkar Marathw ada University, Aurangabad under Industry -Institute Partnership Cell of AICTE, New Delhi.
Skills & Expertise
Formulation & development
Dosage form
Molecular Modification
Analytical method development
validation
Phytosome Technology
Solubility enhancement
Standardization of Herbs & Formulation
HPLC
RP -HPLC
UV&RP -HPLC
LCMS -MS
Statistical Process Control (SPC)
Pharmaceutical tablet Production process
Stability indicating assay methoddevelopement
Solid dispersion technique
Buccoadhesive patches
Sustained release matrix tablet
Mucoadhesivebuccal tablet
Gastroretentive drug delivery system
Mouth dissolving tablet
OrodispersibleTablets
Osmotic drug delivery system
Research Interests
Teaching
Administrative
Research
Quality Assurance
Syllabus Framing
Industry-Institute Partnership
Connect With Me
Experience
Assistant Professor -PG
- Permanent 11 Dec 2014 - Till Date 5 year (PG&UG level)
Assistant Professor -UG
- Permanent 10 Septembe 200710 Dec 2014 7 years and 3 months ( UG level)
Lecturer
- ---- 1June 2006 - Jully2007 1 year -UG-level
Education
College Of Pharmacy, FaizpurNorth Maharashtra University, Jalgaon.(M.S)
Anuradha College Of Pharmacy, ChikhliAmaravatiUniversity, Amaravati.(M.S.)
Anuradha College Of Pharmacy, Chikhli, Buldana.MSBTE,Mumbai.
Bhagawant University, Ajmer
Thesis Guided (30)
Formulation and evaluation of sustained release matrix tablet of Gliclazide
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Formulation and evaluation of mucoadhesivebuccal tablet of propanalol hydrochloride
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Formulation and evaluation of Ambroxyl hydrochloride & salbutamol sulphate sustained release matrix tablet
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Formulation and evaluation of buccoadhesive patches of valsartan
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Solubility enhancement of poorly water soluble drug atrorvastatin calcium by solid dispersion technique using natural carrier
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Solid self emulsif ying drug delivery system of poorly water soluble active constituent curcumin
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Development &Validation of analytical method for simultaneous estimation of omeprazole &Dompiridone in bulk &solid tablet dosage form
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Validated stability indicating assay methoddevelopement for simultaneous estimation of ofloxacin&Nitazoxanide in bulk and its pharmaceutical liquid dosage form
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Development &Validation of rphplc&uv -visible spectrophotometric methods for simultane ous estimation of pregabalin and aceclofenac in tablet dosage form
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Analytical method development and validation estimation of protein impurify in H. InflunzaeType.B polysaccharides by lowery method
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Formulation, development and evaluation of modified release capsule of cyclobenzaprine
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Development and validation of simultaneous estimation method of metronidazole &Norfloxacin &their formulation by Rp -HPLC
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Formulation and evaluation of mouth dissolving tablet of nimodeping
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Design and evalution of Gastro -retentive delivery system for controlled release of anti -ulcer drug
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Formulation and evaluation of osmotic drug delivery system of Zolpidem
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Process Validation Chlorthalidone tablets USP 25mg
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Formulation &Evalution of OrodispersibleTablets of tramadol hydrochloride using novel co -processed superdisintegrants
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UV&RP -HPLC MethodeDeveloment& Validation of DaclatasvirDihydrocloride in bulk drug& formulation
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Formulation &Evalution of Phytosomes of Ficusracemosa Stem Bark
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Delelopment& Validation of some Analytical Methods For estimation of Zopiclone in Bulk &Formulation
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Statistical Process Control (SPC) study on Pharmaceutical tablet Production process for Continous quality Improvement
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Bioanylitical method development and validation of quinine in humn plasma by LCMS -MS
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Formulation &Evalution of MucoadhesiveBuccal film Containing drug
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HPLC Mehtod development , validation & use fexofenadine hcl& its stability studies
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Formulation &evalution of polymer base microneedle for transdermal drug delivery system
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Analytical method development &validation of carvediolol by RP -HPLC -IR in Bulk & Formulation
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Analytical method development &validation of Nimodipine by RP -HPLCIR in Bulk & Formulation
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Formulation of mouth dissolving tablet of Nifedipine&itsevalution
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Formulation & Evalution of floating in situ gel of ranitidine for Gastroretentive drug delivery system
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Standerdization & Analytical Estimmation of different parts of Moringa oliefera linn
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Professional Memberships (1)
Association of Pharmaceutical Teachers of India
Publications (10)
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