RegDesk is a Regulatory Information Management System (RIMS) that helps medical device companies manage global regulatory submissions, product registrations, and compliance in one centralized platform. It streamlines regulatory workflows, organizes regulatory data, and provides global regulatory intelligence to help teams navigate complex requirements across multiple markets. Regulatory affairs and quality teams benefit by reducing manual work, improving submission accuracy, and accelerating time to market.
Our capabilities are as follows:
• AI Application Builder
• Regulatory Intelligence
• Change Assessment
• Standards Management
• Country-Specific Templates
• Distributor Collaboration
• AI Document Management
• Tracking & Reporting
• Alerts and Notification
• Product Management
• Claims Management
• EUDAMED
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Interfacing’s Integrated Management System (IMS) is an AI-powered platform that unifies BPM, QMS, Document Control, and GRC into one platform. Organizations use IMS to model and automate processes, control documents, manage risks, and maintain regulatory compliance with full traceability and audit readiness.
Built for highly regulated sectors such as aerospace, life sciences, finance, and government, IMS provides real-time visibility, automated workflows, and AI-driven insights that improve quality and reduce operational risk. The platform is ISO 27001 certified and fully validated for 21 CFR Part 11, making it suitable for mission-critical environments requiring strong governance, security, and control. IMS also includes low-code automation, process mining, audit management, training tracking, CAPA workflows, and dashboards to help teams streamline operations and continuously improve. AI strengthens governance, improves accuracy, and reinforces regulatory control.
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SAS Life Science Analytics Framework
Only SAS delivers a single, open, cloud-native statistical computing environment for clinical research with embedded analytic tools, support for data standards, and optional integrated analytic applications. Our analytic foundation for clinical research helps you modernize and deliver new therapies to market faster to improve health. Manage and analyze information in a collaborative platform, streamline processes, and more efficiently deliver trial results to regulatory authorities. Provides a cloud-native, single solution for clinical analysis and submission with everything you need for validation, regulatory compliance, versioning, audit trails, and documentation support. Allows for automation through workflows, support for current and future integrations, and implements and properly manages data standards and controlled terminology. Includes central hub for all incoming data, automated data quality analysis, better data management, and analytical data preparation.
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