The MedTech Ecosystem

Ensure your medical devices meet design requirements and patient needs with validation and verification solutions.

• Accelerate the process of evaluating materials and product safety.
• Reduce the validation effort for testing medical device functionality.
• Verify your compliance with industrial regulations quickly.
• Facilitate cross-disciplinary collaboration and solve underlying design issues early.

Fast-track your medical devices with Medidata, the only eClinical solution that helps you run your trials, engage with patients, sites, and sponsors, and leverage the latest clinical research data.

• Smooth the patient recruitment and study experience before, during, and after clinical studies with unmatched patient centricity.
• Simplify and improve clinical data quality with a unified clinical data management solution.
• Design patient-centric studies with AI intelligence and synthetic control arms.
• Transform clinical operations workflows for a shorter study timeline.

Activate a Total Quality Management (TQM) program to comply with ever-changing regulations to get and maintain market approval, manage risk, and meet patient safety demands.

• Move beyond compliance to full traceability across a unified digital thread.
• Continually innovate across your value network in a Product Lifecycle Management (PLM) collaboration environment.
• Effectively capture customer product usage and risks for post-market surveillance.
• Confidently navigate international, regional, and national standards from IEC, ISO, and WHO to FDA, EU MDR, UKCA, and more.

Sustainably accelerate your operations to minimize deviations and waste with a virtual twin of your plant assets, supply chain, and production processes.

• Digitally model your ideal-state production process to create as-built products to match as-designed products.
• Virtually commission, validate and optimize production lines, workflows, and employee ergonomics.
• Achieve next-gen supply chain resiliency with a fully connected supply chain network.
• Proactively monitor plant equipment maintenance for maximum uptime.

Assess how your medical device performs in the real world and adapt your products as your patient experiences evolve.

• Market products using rich, interactive 3D content experiences.
• Personalize surgical planning with seamless collaboration between device manufacturers, surgeons, and other HCPs.
• Monitor post-market activities to track and reduce the number of adverse events and product recalls.
• Link real-world data (RWD) with clinical trial data (CTD) for effective safety tracking.