Wednesday, 22 March 2017
AUSHADH-2K17: One Day National Conference on "Pharmacoeconomic Shift & Quality of Life" on 25th March, 2017 @ VIPER
Pharma Wisdom Jobs
13:57:00
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Greetings from "Vishnu Institute of Pharmaceutical Educational and Research".
Now VIPER is going to organize its “AUSHADH 2K17" which is scheduled on 25th March, 2017 at college premises. The theme of the conference is “Pharmacoeconomic shift and Quality of life”. The conference has planned an exciting scientific program that intends to share experiences with the delegates, the advances that are currently emerging globally in the economics in relation to quality of life. The scientific program includes Key note address by eminent speakers, plenary lectures, scientific poster and oral (podium) presentations. VIPER intends to invite leaders from pharmaceutical industry, academia and regulators to explore the change that is required for the new breed of pharmacists. We are aware of your contribution in this area and particularly your familiarity with the developments that are currently happening in the Pharmacy Profession in India.
Tuesday, 21 March 2017
Monday, 20 March 2017
Pharm.D - IInd Year UNIVERSITY EXAMINATION PREVIOUS QUESTION PAPERS (2012 to 2016) - JNTU HYDERABAD
Pharma Wisdom Jobs
23:25:00
6
PHARM.D II YEAR QUESTION PAPER - 2012
PHARM.D II YEAR QUESTION PAPER - 2013
PHARM.D II YEAR QUESTION PAPER - 2014
PHARM.D II YEAR QUESTION PAPER - 2015
PHARM.D II YEAR QUESTION PAPER - 2016
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Multiple Vacancies in Quality Department @ Torrent Research Center
Pharma Wisdom Jobs
08:04:00
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Dear Candidate,
Greetings from Torrent
Research Center
This is to inform that we
have Multiple Vacancies for Quality Dept.
Designation: Scientist-II
Department: Quality (RA)
Please find the Job
Description given below:
- - To review PDR, MFC, IPS,
specification and STPs of KSM, RM, intermediates and final API
- - To review the technology,
transfer documents like STPs, method validation protocol and report,
characterization data, raw material specification, packaging material
specification, finished product specification, stability. protocol and MPDs
- - To review the manufacturing
documents like MFC, BMR, BPR, process validation protocol/report, stability
protocol/report, sampling protocol, process validation protocol and product
development report
- - To review and evaluate documents
facilitates its usage for commercial purpose of API/KSM/Intermediates.
- - To review outsourced DMF
review for all market such as US, EU, Brazil, ROW etc.
- - To compile amendments,
annual reports, DMF / CEP as per the regulatory guidelines and take care of DMF
extension
- - To evaluate the queries
raised by Regulatory Authority and prepare draft response
- - To initiate and assess
change control and validation form
- - To evaluate API G1 report,
brazil regularization, eCTD publishing
- - To evaluate change
notification/its impact for all market
- - To communicate with vendor
for API related issue
Interested candidates are
requested to send their updated CV on this mail Id
With Regards,
Mihir Adhvaryu
Human Resources
Phone: +91-79-239 69100
EXT: 138