Evolving global pharmacovigilance regulations have recently put the spot-light on finding better and quicker ways to measure and assess medicinal product benefit-risk profiles through new requirements and guidelines. 

Quintiles can help you better understand and comply with these changing regulations through our safety aggregate reporting and benefit-risk assessment capabilities. Through our experienced staff, best-in-class processes, and proprietary technology, we are able to deliver medical, scientific and regulatory reports that are timely, insightful, and stand up to regulatory scrutiny.

For information on our pharmacovigilance services, please click here.