Navitas Life Sciences

As experts with more than 150,000 regulatory submissions under our belt, Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

With insights from more than 5 technologies and more than 100 health authorities, 100 associates, 30 executives, and 5 internal consultants, we drive better outcomes for our clients, as proven by our experience handling 35,000 paper, 95,000 eCTD, and 20,000 NeeS submissions.

Consulting ServicesCRORegulatory Information Management