Drug Regulatory affairs proffesional
Resume:
CURRICULUM
CURRICULUM VITAE
NAME : YADAV VIJAY R.
EMAIL : **.*********@*****.***
MOBILE NO : +91-964*******
PERSONEL DETAILS CAREER OBJECTIVE
PERMANENT ADDRESS
Challenging work in a collaborative team environment with strong technical components and exploring
At & Po Nagaria Road, Opp new horizon in the field.
Gopal Sowmil, Hanuman
Street, ACADEMIC RECORD
Dharampur- 396050
Di- Valsad
Examination Institution & Board Month/Year % Marks
Gujarat
Jaipur college of Pharmacy, Jaipur Affliated
Master of
to Rajasthan University of Health Science
Pharmacy Dec-2013 70.00
PRESENT ADDRESS
(Pharmaceutics)
Bhalchandra college of Pharmacy, Pune
C-Block, Gali no. 9 Bachelor of Affliataed to Pune University June-2011 60.23
House no. 1086, 25 Ft Road, Pharmacy
Mukundpur-II
Delhi-110042 R.P.T.P. Science School, V.V.Nagar, Anand,
GSHEB(XIIth) March-2007 59.00
Gujarat
th
D.O.B : 20 Jan, 1990 R.S.P.Vidhayalya, Dharampur, Gujarat
GSHEB(Xth) March-2005 75.25
Age : 25 Years.
COMPUTER KNOWLEDGE
: Male.
Sex Computer Basic : MS Office.
Marital Status:
PROJECT WORK
Unmarried.
Done industrial project of Bachelor of Pharmacy in production department (Tablet compression and
coating ) from Flourish Pharma pvt. Ltd. Daman for 30 days.
Nationality
Done industrial training of Masters of Pharmacy (Pharmaceutics) from Macleods Pharma Pvt. Ltd.
Indian.
Daman For 6 months.
Languages Known
Hindi
AREA OF INTEREST
English
Gujarati Drug Regulatory Affairs
Marathi
Hobbies
PROFESSIONAL EXPOSURE
Reading, Playing, Music,
Doing Exercise. 1 year 2 months as Technical officer in Drug Regulatory Affairs Department in Rihim Pharma
Consultancy Pvt. Ltd, Delhi
JOB PROFILE
Preparation and review of the dossiers as per the current prescribed guidelines of the respective
regulatory authority CDSCO.
Compile the NDA, ANDA Medical Device, Bulk Drug Registration (import devision) document to
be submitted to Regulatory Agency.
Good face value & Two times a week regular visit of CDSCO Head Quarter (Delhi) for file submission
& Query reply.
Registration of Pharmaceuticals in India & Uganda.
CURRICULUM
CURRICULUM VITAE
Provided regulatory guidance and expedite responses to regulatory authorities. Ensured
documentation complies with regulations for submissions.
Review of the quality and analytical data as per the pharmacopoeia, specification, MOA, STP, batch
records, Stability, Finished product data for the purpose of compilation of the dossier.
Review of documents required for regulatory agencies (Viz. Analytical reports, process validation
reports, Process validation Protocol, pharmaceutical development reports, Protocols & stability data).
Preparation of various pharmacological, pre-clinical & toxicological data based on published
literature.
ONLINE PUBLICATION
Emerging Trends in Superdisintegrants and their role in Tablet Release: A Review
Parkinson’s Disease : A Review
Microsphere : A Review
Research Article : Formulation, Development and Evaluation of matrix tablets of Lornoxicam.
Research Article : Formulation, Development and Evaluation of matrix tablets of NSAIDS by using
hydrophilic and hydrophobic polymers
DECLARATION
I hereby declare that the above-mentioned information is true to the best of my knowledge.
Date: 19/3/2015
Place: New Delhi
Contact this candidate