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Navitas Life Sciences is a proven regulatory affairs partner for small to large bio-pharmaceutical companies, providing cost-effective end-to-end regulatory services, with customization of services to suit unique needs. We have successfully delivered 170,000+ Regulatory Submissions to 100+ global Health Authorities. We have helped 200+ Life Sciences companies with 115,000+ eCTD, 20,000+ NeES, and 35,000+ Paper submissions. Our Regulatory Technology and Industry Regulatory Networks help navigate the regulatory landscape, ensuring proactive compliance and enhanced operational efficiency
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