EU MDR 2017/745 Medical Device Classifier

BETA Version

EU MDR 2017/745
Device Classifier Assistant

About me

Definitions

Try MedBoard

ROUTE 1 (SAFE MODE) Insert 'non-invasive device', 'invasive device' or 'active device' and start making decisions based on questions

ROUTE 2 (RESEARCH MODE) Insert intended use / intended purpose of the Medical Device

If you are a Medical Device, In Vitro Diagnostics, Combination Products Manufacturer and need:

Keeping up to date with and stay on top of:

+100 Regulatory Authorities (Countries) Profiles, Requirements and News
+100,000 Market & Clinical Stakeholders (Manufacturers, Hospitals, etc.) Profiles, Data and News
+10,000 Technical Standards Profiles, Updates and News
+50,000 Medical Products Profiles (Medical devices, IVDs, Software & Apps), Data and News

Powerful Search Engine for instant access to information

PMS Automation & Vigilance

Automate completely Vigilance & PMS into many curated databases and meet easily EU MDR / IVDR requirements

Regulatory & Quality Tools

WW Regulations and Requirements navigation, GAP Analyses, Changes trackers, and much more

Analytics, Insights & Trends

Use RWE data and statistics to feed into your Design Inputs, Risk Management and Intelligence

Clinical and Regulatory databases

WW Clinical Trials, Approvals, Recalls, FSCAs, Adverse Events, Literature, Guidance, and much more for Medical Devices and Pharma

Product Registrations trackers and IM

Regulatory & Competitive Intelligence

Technical Standards Management

Periodic Reports and Full Customization

Starting from only £329/month for Organizations

Disruptive, Innovative, Powerful, Unique, Essential