SAGI brings together your CRM, documents, deadlines and expert workflows to coordinate every team, from regulatory strategy to commercialization.
Every team works from the same information: regulatory strategy, clinical evidence, market access, hospitals, contacts and upcoming milestones.
Track technical documentation, ISO 14971 risk management, CAPAs and supplier audits in one place.
Request accessRequirements, specifications and design reviews linked to the evidence behind them.
Request accessCoordinate CE, UK and FDA pathways, notified bodies, submissions and deadlines across markets.
Request accessHospitals, prescribers and territory pipelines built around long MedTech sales cycles.
Find the right experts and centers, attend the right conferences and keep your medical messaging consistent.
Track recruitment by site, comparative endpoints and post-market follow-up data.
Request accessReimbursement, hospital procurement or direct payment: every market has its own rules and pathways.
Launch an expert-reviewed workflow, adapt it to your device and let SAGI coordinate the steps, documents, owners and deadlines.
Integrate leading AI models
Regulatory clearance, market access or commercial rollout: start from an expert plan and adapt it to your device and market.
SAGI structures work around European and U.S. requirements, with action traceability, document management and access control.
