Discover key considerations in securing medical device regulatory approval and maintaining compliance

Unfortunately we don't fully support your browser. If you have the option to, please upgrade to a newer version or use Mozilla Firefox, Microsoft Edge, Google Chrome, or Safari 14 or newer. If you are unable to, and need support, please send us your feedback.
We'd appreciate your feedback on this new experience.Tell us what you think(opens in new tab/window)
Medical Devices
Medical device companies need to base research and business decisions on high-quality data. Elsevier provides comprehensive coverage of medical device literature and regulatory documents.
R&D organizations are under business pressure to accelerate the innovation cycle in areas such as healthcare equipment and medical device technology. We improve outcomes by illuminating and transforming scientifically validated data at every stage of the innovation workflow.
Improving effectiveness: Scientific insights lead to actionable decisions and meet market demand
Reducing risk: Ensuring companies have the information they need to avoid patent infringement or late failing projects
Maximizing efficiency: Innovate faster, optimize production, reduce costs and eliminate downtime
Created for expert users to provide access to evidence on which to make critical decisions. Either stand alone or integrated into your ecosystem.
Learn more about User Tools.
With career backgrounds in data science, informatics, chemistry, pre-clinical research, clinical development and information management, our experience in industry-standard taxonomies and custom data curation enables us to address your complex data challenges — and help you make better decisions.
Learn more about Expert Support.