Our services

Several ways to work together

From designing an eCOA instrument to validating a regulatory dossier, Bvoxia secures the patient voice throughout your clinical studies.

From one-off advisory to ongoing support, each service adapts to your project's maturity and the place you give to the patient voice.

Acronyms (eCOA, PED, MDR…) are explained in the glossary.

Our services

A short engagement to secure your patient-measurement choices upfront, before locking endpoints and contracting a tool.

  • Framing the patient-measurement need from your protocol
  • Recommendation of validated instruments, fully independent
  • Critical view on the planned eCOA and candidate vendors
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A workshop where real patients, prepared to collaborate with industry, inform your design decisions.

  • Focus-group workshop(s) with patients and the project team
  • Prioritised patient needs and actionable design recommendations
  • Optional extension to a full sprint with functional mock-ups
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A rare, bilingual expertise to strengthen the patient sections of your dossiers — complementing a law firm, not replacing it.

  • Critical review of the patient sections (PRO / COA / PED) before submission
  • Anticipating evaluators' points of attention
  • Commented PED regulatory watch
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Anchor patient engagement durably in your teams, with the same PharmD lead who already knows your context.

  • A regular point of contact on your patient topics
  • Access to the patient-partner network
  • Commented regulatory watch (PED, MDR, AI Act)
Discuss this service

Which service for which need?

Mapping your needs to Bvoxia services
Your situation Recommended service
You start from a protocol and must choose your patient measures eCOA/COA Strategy
You are building a digital tool and want the patient voice Patient × Digital Co-Design
You are preparing an EMA/HTA dossier to secure Patient Data Regulatory
You want expert support over time Patient-Centric Retainer