Our AI/ML engine creates consistent, structured metadata throughout our connected databases, allowing you to research numerous sources simultaneously.
Aggregated, global clinical trial information from ClinicalTrials.gov, EU CTR, ANZCTR, and more.
Research and discover innovative companies and the people behind them.
Premarket notifications by a company that they intend to market a medical device, which must be filed 90 days prior to the device being marketed.
Medical devices grouped into regulatory classes based on intended use and indications for use.
Medical device correction or removal actions initiated by a firm prior to review by the FDA.
Adverse event and medication error reports associated with the use of a drug or biologic product. (FAERS)
Information about drugs, including biological products, approved for human use in the United States.
Medical device reports (MDRs) submitted to the FDA by mandatory and voluntary reporters. One of the FDA's several important postmarket surveillance data sources.
Evaluation of the safety and effectiveness of Class III medical devices.
Locations of medical device establishments and the devices manufactured there.
Collected grant data from sources including Grants.gov, Horizon 2020, NIH Reporter, NSF, SBIR, and Wellcome.
Aggregated data from the UK's Medicines and Healthcare products Regulatory Agency that ensures medical devices, medicines, and blood for transfusions meet standards.
Aggregated business news from thousands of global sources with a focus on science, technology, engineering, and mathematics.
The most up-to-date patent information from all over the world including USPTO, EPO, and WIPO.
Information on chemicals mentioned in Publications and Patents, including 2D and 3D diagrams.
The latest scientific papers from PubMed and preprints from arXiv. BioRxiv, and medRxiv.
Technology transfer opportunities from over 300 research universities around the world.