Key Features
01
Product & Batch Inventory
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​Maintain efficient documentation of device lifecycle information, such as manufacturing dates, expiration dates, and recall statuses, facilitating streamlined inventory management.
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With customizable alerts and notifications, users can stay informed about inventory changes, upcoming expirations, and regulatory updates, ensuring proactive compliance and effective risk mitigation strategies.
02
Submissions Registry
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Keep your regulatory submissions for medical devices and drugs organized and up-to-date with our platform.
Maintain regulatory compliance by keeping up to date registrations and upcoming deadlines.
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Say goodbye to the hassle of managing multiple submissions and stay on top of your regulatory requirements with ease.
03
Custom Dashboard & Reports
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Dynamic dashboard and customizable widgets, allowing regulatory affairs professionals to tailor their view according to their specific needs.
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Users can effortlessly monitor submission statuses, track key milestones, and visualize upcoming deadlines in real-time, facilitating proactive regulatory management.
05
Resources
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Access a pool of industry helpful links to regulatory guidance documents, guides, and other global regulations around the world.
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Search by keyword, topic, or region to find information you need quickly and efficiently.
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Stay up-to-date with the latest industry trends and enhance your regulatory knowledge and expertise
04
Document Management
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Upload, organize, and store regulatory documents.
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Access to industry templates anytime, anywhere, securely print, edit, & share documents with colleagues or regulatory authorities as needed.
06
Projects
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Facilitate teamwork with a platform that enables secure sharing and collaboration among team members.
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Work together seamlessly on regulatory strategies, submissions, and compliance activities.
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Create new projects, tasks, and reminders to help you keep your daily activities in one place.
07
Quality Management
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Centralized repository for quality documents.
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Version control and document history tracking.
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Manage quality events, such as, non-conformances and corrective actions.
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Tracking and monitoring of audit actions and closure.
08
Account Support
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24/7 assistance to help with set-up and ongoing account management.
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Our team is dedicated to providing you with the support you need every step of the way.
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Enter support requests directly within the application to help you keep track of your requests.
Simplified Regulatory and Quality information
Trinity ReguMed Insight was developed to offer more than just a regulatory information database. It’s a holistic platform that supports the strategic and operational needs of regulatory affairs, quality compliance, project management, document management, and product inventory. Whether it’s strategizing for new market entries, managing regulatory submissions, or ensuring ongoing product compliance, Trinity ReguMed Insight provides the tools and insights necessary to succeed.