eCOA/COA Strategy
Start from your protocol to select the right patient-reported measures (PRO/COA), validate their fit and secure your eCOA tool choice.
Learn moreDigital health · Patient-centric
The patient voice,
while it can still shape the outcome.
Bvoxia helps pharma, biotech and medtech with eCOA/COA strategy, patient × digital co-design and patient data compliance — from idea to adoption.
France · Europe — Pharma · Biotech · MedTech / SaMD
Founded by Basile Trimbur, Doctor of Pharmacy (PharmD), 5 years dedicated to eCOA
Drug science and hands-on patient measurement practice, in a single point of contact.
More about the approachMeasuring what truly matters to patients is hard
Ill-suited eCOA solutions, patient data fragile under regulation, tools designed without the voice of their users: digital health projects rarely fail on technology alone.
Bvoxia puts the patient back at the centre — for truly adopted solutions, solid data and dossiers that stand up to evaluation.
PharmD
Doctor of Pharmacy
5 yrs
dedicated eCOA expertise
FR · EU
France & Europe
4
regulatory frameworks (PED, MDR, IVDR, AI Act)
Our services
Several ways to work together
From one-off advisory to ongoing support, depending on your project's maturity.
Patient × Digital Co-Design
Bring real patients and your team together to turn the patient experience into documented design decisions.
Learn morePatient Data Regulatory
Turn Patient Experience Data (PED, EMA/HTA) requirements into concrete actions: critical dossier review and watch.
Learn morePatient-Centric Retainer
Your outsourced patient-engagement lead, a few days a month, without hiring a full-time role.
Learn moreWhy Bvoxia?
Leading expertise, a human approach
A rare expertise
Doctor of Pharmacy (PharmD) with 5 years dedicated to eCOA: drug science and field practice combined.
Patient collaboration, in practice
Co-design workshops with patient associations and many expert patients (EUPATI-trained); Basile regularly attends leading conferences such as Patients as Partners: the patient voice shapes every decision.
Regulatory built-in
PED EMA/HTA, MDR, IVDR, AI Act considered upfront — for projects robust under evaluation.
Agile and committed
A single expert point of contact, committed to your goals with the agility of a human-scale structure.
Our approach
From patient to deployment
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Start from the patient experience
Understand real-world use, needs and barriers.
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Co-design
Align patient need, digital feasibility and clinical goals.
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Frame the regulatory
Embed compliance and acceptability from the start.
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Deploy & anchor
Equip and train your teams for durable adoption.
A digital solution project for your patients?
Let's talk about your goals. First contact with no commitment: reply within 2 business days, quote within 5 business days.
Get in touch