About This Business

Essenvia is a MedTech Regulatory Information Management (RIM) Platform designed to streamline regulatory workflows across the total product lifecycle. By leveraging Essenvia's platform, companies can accelerate global market access and generate exponential business value. The platform is tailored to meet the needs of various stakeholders, including Vice Presidents, Heads, and Directors of Regulatory Affairs, as well as Specialists and Managers of Regulatory Affairs. For regulatory affairs leaders, Essenvia offers modern RIM technology that drives business value and brings cross-functional efficiency gains to all teams and departments, including Regulatory Affairs, Quality Assurance, Research and Development, and Project Management Offices. This empowerment enables the acceleration of product launches and the elimination of revenue loss due to submission delays and missed renewals. The platform provides a helicopter view of the total regulatory lifecycle, complete with executive dashboards, metrics, and proactive alerts for global registrations, submissions, and change assessments. For specialists and managers, Essenvia offers a comprehensive overview of the regulatory cycle, including dashboards and progress metrics on global registrations, submissions, and change management, along with alerts and notifications. Essenvia's mission is to help MedTech companies worldwide achieve regulatory excellence and bring their products to market faster. With its headquarters located in Los Angeles, California, Essenvia is committed to supporting its clients through personalized demos, support services, and connectivity with its team. By trusting Essenvia, MedTech companies can optimize their regulatory operations, enhance their competitive edge, and ultimately improve patient outcomes through faster access to innovative medical technologies.