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Pharmacovigilance assume a significant part in the medical services framework through checking and connection of medications and there impacts in the human body. In this article a overview on Drug safety processes i.e. an look on the Pharmacovigilance department with (GCP) and (ICH) rules for drugs for human use are inspected as a significant viewpoints in the change of clinical trial to the goal of Pharmacovigilance In drug creation India turns out to be third biggest country on the planet. These days in India Pharmacovigilance gives mindfulness about adverse medication responses (ADR) and this survey gives data about the basic Pharmacovigilance processes and concepts of data management.

KEY WORDS:

 Pharmacovigilance, Adverse Drug Reaction, Data Management, ICH, ADR Assement.