The B.E. Centre (ISO 9001:2000) had been carrying out Bioequivalence study most satisfactorily since 2002 being approved by DCGI Oct-2002.

What's New

A SHORT TERM TRAINING COURSE ON

"BIOEQUIVALENCE STUDY OF DRUG BY HPLC"

ABOUT THE COURSE
A Short term training course will be held on “Bioequivalence  Study of Drug by HPLC” where distinguished speakers of repute from the centre as well as from outside organizations will be interacting with the participants.


OBJECTIVES
The course has been designed for the students of Under Graduate & Post Graduate level having pharmacy, biology and science background. The course will illustrate not only the theoretical back ground of biopharmaceutics but also it will render the practical exposure to various instrumental techniques very much fitted to the syllabus of pharmacy course and to the requirement of pharma industry.

ELIGIBILITY CRITERIA FOR PARTICIPANTS
B.Pharm/ M.Pharm/ Students of M.Pharm/ 3rd  & 4th year B.Pharm./ B.Sc / M.Sc/ Students of M.B.B.S.
Industry/Institute sponsored candidates are also eligible for the course.
Registration fee:
Students: Rs. 8000/-
Industry/Institute Sponsored candidate: Rs. 10,000/-
The payment may be paid by cash or DD drawn in favour of “Clinical Research Pharm Tech” Payable at Kolkata.

 

 

FOURTH BATCH

Date of Commencement: 1st week of February, 2012

Timing: Saturdays/ Sundays
Total Duration: 4 Days
Total Time: 25 hrs.
Course Fee: Rs. 8000/-
Available seats: 20 persons (First come first serve basis)
Course Director: Prof. (Dr.)T K.Pal
Course Co-ordinators: Prof. (Dr.) S. G. Dastider
Mr. Amlan Kanti Sarkar (M) 9062524987
Mrs. Bhaswati Gupta (M) 9830089297

DOWNLOAD REGISTRATION FORM

Email:- tkpal12@gmail.com

 

 
FOCUS

Exposure to the sophisticated instruments like HPLC, Automated Dissolution Apparatus etc. utilized in Pharmaceutical Industries.

  • Hands on practical experience on HPLC .
  • Challenges in analytical method development of drug by HPLC in Human Plasma
  • Biostatistical analysis of pharmacokinetic parameters.

Course Content

Duration

Basic concept of Bioequivalence Study Design
(as per Central Drugs Standard Control Organization, Govt. of India)/Volunteer screening/Drug Administration/ Blood Sampling/ Processing & Storage of blood plasma/ SOP

5 hrs.

Basic concept of HPLC/ SOPs for HPLC/ Method Development, Calibration & Validation in HPLC/ Analysis of Drugs in Plasma
(Theoretical / Practical)

20 hrs.

 

Last date of registration: 31st January, 2012.
The registration form will be available from
BIOEQUIVALENCE STUDY CENTRE
DEPARTMENT OF PHARMACEYTICAL TECHNOLOGY
JADAVPUR UNIVERSITY
KOLKATA – 700 032.

FOR REGISTRATION FORM LOG ON TO  www.biostudy.in

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