.svg){kind=logo}
Regulatory submissions are not managed together.
Centralize the processes with Approvia.
Structure your FDA submission, then let Approvia handle automated review assignments and focus tasks across multiple departments.
Approvia is designed to be customized to your standard operating procedures, which prevents your users from adopting clunky workarounds or switching between multiple applications.
Our novel approach to review and approval assignments allows your external stakeholders to securely contribute to documents, without the need for a login or password.
Approvia's granular audit logs ensure your application and regulatory submission documents follow FDA guidelines, eliminating the risk of delays or rejection.
Approvia offers the perfect balance of pre-built functionality and flexibility, with 80% of the solution already built and the remaining 20% configured to your unique requirements.
This means you get the speed and affordability you need, plus powerful customization options not available in competing regulatory affairs management software.
Our flexible, scalable process automation solutions empower medical affairs teams at life science organizations to operate better and do their best possible work.
