Successfully navigate complex regulatory requirements

Bring transparency, efficiency and predictability to your regulatory affairs strategy by outsourcing to IQVIA.

Our global regulatory scientists use a proprietary Regulatory Information Management (RIM) solution powered by a centralized regulatory intelligence database and BPM tools to provide compliance and increase value for your product. We bring people and technology together to tackle your most challenging issues:

  • Submitting multi-layered NDAs and MAAs
  • Executing label changes across several countries
  • Managing the ebb and flow of regulatory needs as you grow
Securing speciality drug designations faster than the competition.

Reach out today to achieve peace of mind in regulatory affairs.

Regulatory Affairs

Medical Writing and Document Publishing
IQVIA offers a range of flexible medical writing and document publishing solutions to support many types of study needs, giving you the quality and timeliness that can keep your project on track.