Home Solutions Life sciences MedTech MedTech Regulatory intelligence for MedTech Infodesk helps MedTech organizations manage regulatory complexity with confidence. Across medical devices, diagnostics, and digital health, our regulatory intelligence supports faster responses, reduced risk, and defensible decisions throughout the product lifecycle. Book a meeting The challenges slowing down MedTech teams MedTech organizations operate under intense regulatory pressure, growing cybersecurity risk, and constrained resources. Regulatory intelligence plays a critical role in helping teams manage complexity, coordinate faster, and maintain compliance as expectations continue to rise. Regulatory compliance and complexity MedTech companies must navigate strict and evolving frameworks such as EU MDR, IVDR, and upcoming quality system requirements. Manual surveillance makes it difficult to track change, interpret impact, and maintain audit readiness across global markets. Rising volume and pace of change Regulators issue more guidance, updates, and commentary than ever before. Without structured monitoring, teams risk missing changes that affect development timelines, approvals, or post-market obligations. Information overload and blind spots Updates arrive through disconnected emails, alerts, and third-party sources. Without filtering, validation, or shared visibility, critical regulatory intelligence is buried, delayed, or lost. Slow and inconsistent communication Even when changes are identified, they’re not always shared with the right teams at the right time. This slows assessments, creates gaps between QA, RA, and legal, and increases compliance exposure. Disconnected workflows Impact assessments, documentation, and post-market activities often sit across separate tools. This adds manual effort and makes it harder to maintain traceability under audit scrutiny. Cybersecurity pressure Connected devices, software-driven products, and digital health tools increase exposure to cyber risk. MedTech organizations must stay alert to emerging threats while ensuring the systems they rely on are secure and defensible. Quality and post-market burden Maintaining an audit-ready quality system is time-intensive, especially for companies with products already on the market. Post-market surveillance demands structure, coordination, and reliable records without adding administrative strain. Built for how you work MedTech organizations manage regulatory change, cybersecurity risk, and quality expectations across devices, software, diagnostics, and global markets. Infodesk supports faster assessments, better coordination, and regulatory intelligence that holds up under pressure. Track MDR, IVDR, and global regulatory change with validated updates Create structured cases for faster, more consistent impact assessments Share regulatory and safety updates across QA, RA, and legal from one place Maintain audit-ready records that support quality and post-market obligations Strengthen visibility into emerging cybersecurity risks affecting connected technologies Why MedTech teams choose Infodesk Faster, more confident decisions Curated, validated intelligence reduces manual surveillance and helps teams respond quickly to regulatory developments that affect development, approval, and compliance. Clear strategic visibility Centralized monitoring brings regulatory updates, scientific developments, and market signals together, reducing blind spots across regions and product areas. Reliable traceability Every update, assessment, and decision is supported by source history and context, creating defensible records for audits, inspections, and internal review. Better coordination across functions Shared views and structured workflows keep QA, RA, legal, and leadership aligned, reducing delays and fragmented communication. Stronger cybersecurity awareness Early visibility into emerging cyber risks helps teams stay alert to threats affecting software, connected devices, and digital health products. Greater resource efficiency Structured workflows and reduced manual effort help teams focus limited resources on higher value regulatory, quality, and innovation work. More ways to work with Infodesk Regulatory Workflow Solution Turn updates into action with structured case management, SME tracking, audit-ready records, and real-time visibility – purpose-built for regulatory, quality, and safety teams. Read more Market intelligence Infodesk unifies global market and competitive intelligence, combining AI and analyst validation to deliver timely, verified insights for faster decisions Read more Regulatory intelligence Filter scientific updates by topic, region, or therapeutic area and deliver credible research to stakeholders at speed, with full source transparency Read more Intelligence activation for Life Science customer stories View all stories Automating pharmacovigilance workflows for compliance with Health Canada’s Foreign Risk guidance 73% Time saved Infodesk provided a user-friendly dashboard with curated information, empowering the team to overcome the challenges of information overload. Not only… Read case study Company-wide access to current drug pipeline research on-demand 50% Time saved Developing an AI-powered curated solution to monitor the regulatory landscape Efficiently monitoring the latest scientific literature by automating Medical Affairs workflows 80% Time saved Learn how this medical affairs team at a global pharmaceutical organization use Infodesk’s automation and expert curation to share critical… Read case study $62BN The costs of not managing regulatory surveillance Empowering the quality division: optimizing GxP Regulatory Intelligence in pharmaceuticals Discover more about the Infodesk platform From intelligence to impact. The Infodesk platform drives informed action for enterprises Monitor You can’t confidently manage what you don’t monitor. Infodesk’s surveillance and monitoring capabilities keep you informed and in control Curate With AI-powered curation features, Infodesk helps organizations turn complex, high-volume information into decisive, auditable action. Action Where intelligence means impact. Infodesk helps convert intelligence into outcomes Trusted scientific and regulatory content From policy shifts to safety events, Infodesk delivers validated, compliance-focused intelligence from the sources your teams already rely on. Find out more Managed professional services Alongside Infodesk’s monitoring features, our team of analysts, editors, and information specialists combine human expertise with advanced technology to deliver trusted, relevant intelligence. All without added effort on your part. Their oversight ensures intelligence is validated, curated, and always aligned with your priorities. With backgrounds in analysis, research, journalism, communications, and publishing, our experts act as an extension of your team. They provide timely intelligence that’s ready to use, helping your organization respond faster, reduce manual work, and focus on high-value strategic decisions. Find out more Human first, always We use AI to elevate human judgment, not to replace it. In high-pressure environments, explainability matters as much as efficiency. Blogs and Insights View all insights Insights Harnessing regulatory intelligence surveillance for strategic advantage Read more Insights Brochure regulatory affairs leaders Read more Blogs Insights from the Regulatory Customer Forum: Turning Regulatory Intelligence into Action Read more Case Studies Staying on top of the regulatory landscape with real-time information Read more Blogs Regulatory Intelligence Forum: From Insight to Impact with Experts from Pfizer, AstraZeneca and Haleon Read more Insights Regulatory workflow solution Read more