Pharmacovigilance - Driving Safety

Pharmacovigilance, the monitoring of the quality, safety, and efficacy of marketed medicines, is critical to the long-term success of every drug. Today, manufacturers and marketers are held accountable for any and all reports of adverse drug reactions, and other safety-related events.

Due to the global demand for improved public health, regulatory agencies monitor drug safety constantly and closely. The late 1990s alone saw 15 drug recalls—a devastating happenstance for a pharmaceutical or biotech company in terms of financial loss, credibility, and image.

Life sciences companies need to have systems and processes that preempt monitoring drug safety and report periodically to regulatory agencies. This can be done by collecting and analyzing data to ensure safety using technology solutions. The right solutions provide scalability and consistency, despite massive increases in safety data (variety of drugs, number of patients, number of adverse events, etc.).

We have helped life sciences companies monitor the safety and efficacy of their products while working towards solving some of their most challenging clinical safety issues. In short, we help clients manage safety issues.

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