Several ways to work together

A framing engagement to start on solid, measurable and compliant foundations.

• Audit of the existing setup: instruments, data flows and friction points
• Recommendation of validated instruments (PRO / ObsRO / ClinRO) suited to your protocol
• Secure paper → electronic migration plan
• Scoping of linguistic and regulatory validation requirements

Format: short engagement · 3 to 7 days · fully remote possible

An intensive format that turns a real need into a testable prototype, with patients.

• Co-design workshops with patients and teams
• Mapping of the patient journey and real needs
• Testable prototype of the digital tool
• Prioritised roadmap for what comes next

Format: sprint · 4 to 8 weeks · one-off workshop possible (1-2 days)

Anticipate European requirements rather than endure them, and secure your dossiers.

• MDR / IVDR and Patient Experience Data (EMA) compliance analysis
• Anticipation of HTA expectations and the AI Act
• Risk mapping and compliance roadmap
• Support in building and reviewing dossiers

Format: dossier review in days · PED production over 2-3 months · bilingual FR/EN

Patient-centric expertise available over time, embedded with your teams.

• Patient-centric expertise available on an ongoing basis
• Upskilling of your teams
• Consistency of decisions and trade-offs over time
• Regular check-ins and priority access

Format: monthly support · 6 to 12 months, renewable