IQVIA Regulatory Affairs And Drug Development Solutions

Life sciences organizations are often strained by the demand of regulatory complexity and maintaining compliance in different geographies. In addition, keeping up with the ever-changing regulatory landscape can be time-consuming and costly.

IQVIA provides regulatory, scientific, and medical advisory services (e.g., TPPs, CDPs, synopses, indication prioritization, and asset valuation) supported by our data and technology to enhance customer journeys from early drug development through submissions and post-registration.