Regulatory Submissions, Information, and Document Management Forum

Reduce Time, Cost, and Risk, from Drug Discovery Through Post-Registration

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 in the drug development continuum.

Learn how IQVIA’s Regulatory Affairs and Drug Development Solutions (RADDS) provides data-driven strategic drug development and technology-enabled services to drive efficiency in regulatory affairs, operations, submissions, and regulatory intelligence along the entire lifecycle of the product.

• Regulatory strategy across the entire drug development continuum
• Maximize early strategic advantages to enable operational efficiency
• Enhance regulatory affairs from pre-registration to post-registration
• Use AI/ML and regulatory intelligence tools to lower administrative burdens