E-DRUG: Short program on Pharmacovigilance and Drug Monitoring
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MDP on "Pharmacovigilance and Drug Monitoring " October 30 - November 3,
2017*
Pharmacovigilance is the process of monitoring and enabling an environment
for the control of adverse drug reaction. There is a need to strengthen the
Pharmacovigilance system and make it beneficiary to the population,
understanding various aspects of Pharmacovigilance is essential as the
treatments are monitored for their safety and effectiveness under real-life
conditions post-market release. The program is going to emphasize upon
Pharmacovigilance information into action, describe and analyze the
risk/benefit, economics of drug use and to advise for decision making.
Major program contents
- Current status & issues of Post-marketing studies Adverse event (AE),
reporting procedures, risk/benefit analysis for the use of medicines
- Design of Post-marketing studies
- Reporting Guidelines
- Spontaneous Reporting
- Prescription event monitoring
- Drug utilization studies
- Signal Detection & Analysis
- Causality assessment of adverse event
- Drug Coding & PV Data Management
- Periodic Safety Update Report
- Setting-up of PV center & Operationalization
- ICH- GCP Guidelines & Global PV Regulation
The program will be organized in IIHMR University, Jaipur, India which is
ranked No. 1 B-School in Health Sector in India (Outlook Magazine). The
Institute has been designated as WHO Collaborating Center for District
Health Systems based on Primary Health Care. The Ministry of Health and
Family Welfare, Government of India has identified the institute as an
Institute of Excellence for training and capacity building.
For more details please go through the Brochure
<https://iihmr.edu.in/pages/download?file=app/webroot/files/training/brochure/92/operation-management-2017.pdf>
& official web page
<https://iihmr.edu.in/trainings>
regarding the program.
Regards
Rahul Sharma
Program Coordinator
IIHMR University, Jaipur, India
rahul sharma <rahulsharma1in@gmail.com>