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Solutions Product Registrations Submissions Medical Device UDI Standards Management Essential Principles Regulatory Intelligence Products Rimsys Platform UDI Integrations Pricing Customers Resources Library Blog Events Regulatory market profiles Regulatory performance report Medtech industry news Get a demo Get a demo Solutions Product Registrations Submissions Medical Device UDI Standards Management Essential Principles Regulatory Intelligence Products Rimsys Platform UDI Integrations Pricing Customers Resources Library Blog Events Regulatory market profiles Regulatory performance report Medtech industry news Get a demo Get a demo Solutions Product Registrations Submissions Medical Device UDI Standards Management Essential Principles Regulatory Intelligence Products Rimsys Platform UDI Integrations Pricing Customers Resources Library Blog Events Regulatory market profiles Regulatory performance report Medtech industry news Get a demo Get a demo Solutions Product Registrations Submissions Medical Device UDI Standards Management Essential Principles Regulatory Intelligence Products Rimsys Platform UDI Integrations Pricing Customers Resources Library Blog Events Regulatory market profiles Regulatory performance report Medtech industry news Get a demo Get a demo TURN REGULATORY INTO REVENUE WITH MEDTECH-FOCUSED RIM SOFTWARE Plan better, execute faster, and ensure global regulatory compliance Learn more EBOOK See how regulatory strategy can be a powerful competitive differentiator The trusted technology partner for medtech regulatory affairs Customer stories THE RIMSYS PLATFORM The Rimsys Regulatory Information Management Platform digitizes and automates regulatory activities in a single cloud-based platform, helping regulatory affairs teams work more efficiently, bring products to market more quickly, and reduce non-compliance risks. CENTRALIZE ALL REGULATORY INFORMATION Create, organize, and consolidate a “single source of truth” for registrations, certificates, submission documents, technical files, UDI, and correspondence with health authorities. Ensure that everyone is working with consistent, up-to-date information. STREAMLINE SUBMISSIONS Collaborate with team members and in-country sponsors to quickly assemble regulatory applications using pre-built digital templates, intelligent reusable content, and automated approval workflows. MONITOR MARKET STATUS Automatically track registration and selling status, expirations, relevant standards, and regulatory news to ensure products can stay on the market without disruption. ALL OF YOUR RA PROCESSES IN ONE INTEGRATED PLATFORM Product registrations Monitor and manage global product registrations, certificates, and expirations Learn more Submissions Collaboratively author and assemble regulatory applications Learn more Unique device identification Manage global UDI information alongside product registrations Learn more Regulatory intelligence Track relevant laws, regulations, guidance, and news Learn more Essential principles Create and maintain essential principles/general safety and performance requirements (GSPR) tables Learn more Standards management Proactively monitor changing global standards Learn more RIMSYS INTEGRATES ACROSS YOUR EXISTING SYSTEMS Easily connect clinical, product, and quality information across your organization. Update market clearance and selling status directly in your ERP or CRM for immediate MDSAP compliance. Explore integrations Want to learn more about Rimsys? Contact us for a free demo Get a demo Contact Rimsys HomePricingCustomersDemo Company AboutCareersContact Support Services & supportHelp centerSecurity & privacyPrivacy policy © 2023 Rimsys. All rights reserved. Resources LibraryBlogEventsRegulatory market profilesRegulatory performance reportMedtech industry news Products Rimsys PlatformUDIIntegrations Solutions Product registrationsSubmissionsMedical device UDIStandards managementEssential principlesRegulatory intelligence