Contact Sales Support Center
A comprehensive solution designed to manage regulatory submissions and eCTD processes.
Streamline submission processes to meet regulatory timelines and bring products to market faster.
Ensure global regulatory compliance with built-in validation checks and standardized workflows.
Manage all regulatory data, documents, and communications in one secure platform.
Facilitate teamwork with tools for simultaneous document reviews, annotations, and task assignments.
Streamline the management of regulatory information with an integrated RIMS. Track product registrations, health authority interactions, and submission timelines in one platform. Improve oversight, ensure data accuracy, and simplify regulatory planning.
ACE RIMS ensures adherence to global submission standards, including FDA, EMA, and other regional health authorities. Automated validation checks guarantee compliance before submission. Expand your global reach with confidence, knowing your submissions meet all regulatory requirements.
Monitor submission milestones and ensure all required documents are accounted for with real-time tracking tools. Notifications keep your team informed about deadlines and document approvals. Avoid delays and ensure submission readiness with precise tracking and alerts.
Enable multiple users to review and annotate documents simultaneously, improving efficiency and reducing errors.
Track changes and ensure all users work on the latest document version to maintain data integrity.
Visualize key regulatory metrics with customizable dashboards and generate actionable reports.
Get answers to your questions and discover how ACE can help you transform your business with regulatory information management.