Innovations and increase in the number of drugs into the market resulted in rise of adverse drug events and drug related toxicities. With the utmost importance on patient safety and regulatory compliance, pharmaceutical firms must effectively monitor and detect adverse event reports and comply with all regulatory standards. Increased public scrutiny has been driving the focus on drug safety surveillance.
Objective
* To understand different aspects of Medical Safety and Pharmacovigilance in practive.
* To Understand issues regarding risks and benefits of drug use in humans including the cause, manifestation and consequences of adverse drug events (ADEs).
* To understand about detection and monitoring of the Adverse Drug Reaction.
* To Understand aspects for Pharmacovigilance compliance and monitoring.
For more detailed information please visits
https://iihmr.edu.in/uploads/brochure/PDM-Brochure.pdf
Nicely written and great info.Thanks to share the more information's.
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Pharmacovigilance is a branch of the pharmacy where vigilance is kept over the use of drugs. According to WHO guidelines, proper reporting of Adverse drug reactions, and Adverse events is necessary in order to completely justify the job of Pharmacovigilance. At present career in it is at boom and various institutes provide Pharmacovigilance courses.
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Excellent information and a well-written article. I appreciate you sharing more details. Currently, careers in it are booming, and several institutions offer courses in pharmacovigilance. Pharmaceutical companies must efficiently monitor and detect adverse event reports and adhere to all regulatory criteria, placing the utmost focus on patient safety and regulatory compliance. With the aid of a clinical research course, there are many opportunities to pursue a career in this field.
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