JAGGAER One · Manufacturing · Medical Devices & MedTech

    Source to Pay Built for
    How Medical Device Procurement Works.


    Click image to enlarge

    Click image to enlarge

    Click image to enlarge

    Click image to enlarge

    Click image to enlarge

    Click image to enlarge

    ISO 13485 supplier qualification

    Onboard and re-qualify suppliers to ISO 13485, 21 CFR 820 and EU MDR with full audit trails.

    Click image to enlarge

    DHF-linked BOM sourcing

    Source against design history file BOMs with engineering change and should-cost integration.

    Click image to enlarge

    SCAR and non-conformance management

    Run supplier corrective actions and closed-loop CAPA workflows within a validated audit trail.

    Click image to enlarge

    UDI traceability and lot tracking

    Track UDI, lot and serial numbers end to end and run EUDAMED and FDA reporting workflows.

    Click image to enlarge

    Contract manufacturer oversight

    Manage sterile manufacturing contracts, quality agreements, tech transfer and site scorecards.

    Click image to enlarge

    NPI sourcing tied to design transfer

    Link sourcing events to stage-gate NPI milestones from prototype through design transfer.

    Click image to enlarge

    Your S2P concierge is here.
    AI grounded in your policies.
    Fluent in your data.

    JAI surfaces where your spend is going off-contract, which suppliers are causing it, and what to do, without you having to build the query.

    JAI · YOUR S2P CONCIERGE

    From the CSCO mapping ISO 13485 tier-n risk to the NPI lead running design transfer. JAGGAER One fits every role in MedTech.

    9%

    84%

    75%

    13M+

    DrägerLife Sciences and Pharma
    • At least 95% of direct order items processed through JAGGAER
    • Order, confirmation, shipping notification and invoicing mapped end to end
    “Dräger rethinks procurement with JAGGAER One.”
    Alexander Bramkamp, Head of Strategic Supply Chain, Dräger~15,000 employees · World market leader in medical & safety technology, Germany
    Learn More
    AlkermesLife Sciences and Pharma
    • $30M in project cost savings delivered through procurement
    • Procurement repositioned as a strategic business enabler
    “Procurement as a strategic business enabler delivered $30M in project cost savings at Alkermes.”
    Rebecca Pender, Alkermes$1.5B annual revenue · Biopharmaceutical company focused on psychiatric & neurological treatments
    Learn More
    LabCentralLife Sciences and Pharma
    • Procurement powers scientific achievement across the labs
    • Streamlined ordering for life-science researchers
    “LabCentral powers scientific achievement through procurement.”
    Victoria Ravenelle, LabCentral$20.6B raised by resident startups · Nonprofit biotech launchpad in Cambridge, MA
    Learn More
    Gartner®

    Magic Quadrant

    • 2026VisionaryS2P Magic Quadrant
    • 2025VisionaryS2P Magic Quadrant
    • 2024VisionaryS2P Magic Quadrant
    IDC MarketScape

    IDC Rankings

    • 2025LeaderCLM & P2P
    • 2025LeaderAI-Enabled Buy-Side CLM within S2P
    • 2025LeaderAI-Enabled P2P Application
    Ardent Partners

    Technology Advisor

    • 2026Market LeaderAutomation & Payments
    • 2024Vanguard LeaderStrategic Sourcing
    • 2023Vanguard LeaderePayables

    Tell us your device class, your CM mix and your biggest qualification pain. We’ll show you exactly where JAGGAER One fits.

    • ISO 13485 & MDR?
      End-to-end supplier qualification with full audit trail.
    • DHF-linked BOMs?
      Design controls, ECOs and specifications on every RFQ.
    • UDI & recalls?
      Tracking, post-market and EUDAMED reporting.
    • Class I, II or III?
      Configured for your device class, not customised.

    JAGGAER One ships with ISO 13485 supplier qualification workflows including audit checklists, evidence collection, scorecards, re-qualification cycles and CAPA workflows. Audit trails meet 21 CFR 820, EU MDR and ISO 14971 expectations.

    Yes. DHF-linked BOMs include design controls, design transfer, ECO / ECR sync from PLM, specifications, drawings and traceability matrices. NPI sourcing is tied to engineering revisions.

    Yes. UDI tracking, lot and serial traceability, recall workflows, post-market surveillance, complaint handling and FDA / EUDAMED reporting are built into the supplier master and procurement workflows.

    CM sourcing covers contracting, quality agreements, change control, tech transfer, capacity planning, sterile manufacturing and packaging. Multi-site oversight and performance scorecards are standard.

    JAGGAER One is configured for Class I, II and III devices, IVDs, combination products, capital equipment and software-as-a-medical-device. Each class inherits the relevant regulations and qualification workflows.