Regulatory & device
openFDA · AccessGUDID · EUDAMED
IntelMed connects manufacturer, device, clinical, tender and safety records into one sourcing workspace, so distribution teams can move from market signal to defensible shortlist without losing the source trail.
Invitation-only access · Built for medical-device distribution and sourcing teams
Example sourcing brief
Illustrative category · Southeast Europe
Recommended next step
Review supplier fit, territory rights and the live tender documents before acting.
Live, source-backed coverage in this workspace
Connected market intelligence
Finding a product is only the beginning. IntelMed keeps demand, readiness, risk and supplier context connected, so a promising signal can become a researched commercial decision instead of another browser tab.
Prioritise
A ranked inbox turns tender demand, clinical movement, regulatory changes, supply gaps and company events into specific next steps for your markets.
Investigate
Search global device records by category, risk class, manufacturer country, market availability, specifications and linked clinical evidence.
Anticipate
Track worldwide device studies, sponsors, sites, lifecycle changes and results to find emerging categories worth deeper diligence.
Validate demand
See public buying activity, delivery markets, deadlines and device categories with a direct route back to the official notice.
Screen risk
Keep FDA recalls, enforcement actions, shortages and discontinuances beside the product record—not in a separate research trail.
Build the shortlist
Connect manufacturers to devices, regulatory progress, markets, funding and distributor coverage before starting a conversation.
From signal to action
IntelMed is built around the decision a distributor needs to make—not around the shape of any single registry.
Evidence stays attached
Open the official record, see when IntelMed observed it, and distinguish a source fact from an inferred opportunity.
01
Define the device categories, territories, regulatory threshold and commercial signals that matter to your distribution business.
02
Move from a ranked signal into the manufacturer, device, clinical, tender and safety context without rebuilding the research trail.
03
Shortlist, dismiss or action the opportunity, then monitor the underlying evidence for changes that could alter the decision.
Provenance by design
Sourcing intelligence is only useful when your team can challenge it. IntelMed preserves the record behind each claim and makes uncertainty explicit.
openFDA · AccessGUDID · EUDAMED
ClinicalTrials.gov · EU clinical investigation reports
TED — Tenders Electronic Daily · public procurement records
FDA recalls · enforcement reports · shortages and discontinuances
IntelMed supports research and supplier discovery. It does not certify devices, establish distribution rights, confirm product availability or replace regulatory and commercial due diligence.
Manufacturer intelligence
Move from a market event to the manufacturer, its product portfolio and the regulatory evidence already on file. These are examples from the current IntelMed dataset.
Greece
0 devices indexed
Profile evidence available in IntelMed
Germany
0 devices indexed
Profile evidence available in IntelMed
Greece
0 devices indexed
Profile evidence available in IntelMed
United States
3 devices indexed
Your next sourcing decision
Bring opportunity discovery, supplier research and source-level diligence into one shared workflow.
Access is managed by invitation.