The evolution of pharmacovigilance in recent years and its growing importance as a science critical to effective clinical practice and public health science have become a significant influence on the drug regulatory authorities, at a time when drug safety concerns have become increasingly important.

The stringent regulations on safety monitoring and their periodical revision have led to increased safety data collection, analysis and regulatory surveillance. To ensure patient safety, minimize costs, and assure compliance, life sciences firms must aggressively detect and manage emerging safety risks. SunBio IT Solutions addresses the evolving issue related to drug safety and adverse drug reactions.

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