Digital batch records
Paper records slow audits. We digitize and version compliance evidence.
PHARMACEUTICAL & HEALTH
Make your pharmaceutical production reliable.
We build tools for the pharmaceutical industry: quality management, batch traceability, GMP compliance and critical process automation. For labs and production sites that demand rigor and traceability.
Prefer to talk before formalizing anything? 20 min by video or over coffee.
Expertise built within demanding organizations.
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Sector specifics
What makes this sector demanding
Pharma experience
Vivien NOEL
Co-founder & technical lead
Delivery & quality
Soraya NOEL
Co-founder & delivery
Available for a 20-min call or coffee before anything is formalized.
YOUR CONTACT
Our experience in pharma and quality
Vivien spent four years at Sanofi R&D on sensitive projects: quality, metadata, pipeline automation, and decision-support tools for research. He understands the compliance, traceability, and documentation stakes for audits.
Soraya leads delivery and coordination. She ensures every deliverable meets deadlines, quality standards, and your teams’ validation processes.
Meet usTypical use cases
Where we secure quality and compliance
Compliance & audits
Deviation and CAPA management
Production deviations are poorly tracked. We centralize corrective actions and evidence.
Raw material-to-finished goods traceability
A recall takes hours to investigate. We reduce that time with online traceability.
Quality dashboard
Quality indicators are scattered. We aggregate them into a real-time dashboard for reviews.
MVP ideas
MVP ideas for pharma
Simulate the impact of a first measurable version before building it.
Digital batch traceability
Track a batch from raw material to finished product and speed up investigations during recalls or audits.
Explore this MVPDeviation and CAPA management
Centralize deviations, investigations and compliance evidence to make inspections easier.
Explore this MVPQMS cockpit
Bring deviations, CAPA and audits into one unified dashboard to anticipate inspections.
Explore this MVPYour topic is not listed?
Let’s talk for 20 min to find the right angle and a measurable first version.
Discuss your projectWhy us
A taskforce that understands pharma
We know the pressure of audits, documentation rigor, and system complexity in the pharmaceutical industry. Vivien brings technical and regulatory expertise. Soraya handles delivery, traceability, and handover to your teams.
Book a 20-min strategy callWe have worked at:
How it works
A clear process, from scope to handover
Scope, timeline and price agreed upfront.
01
Objectives, scope and fixed price
We frame the need, expected deliverables and fixed price together. A contract formalizes the scope and expected results.
02
Delivery with metrics
Measurable increments demonstrated weekly, with a shared dashboard and quality indicators.
03
Validated result = billing
You only pay at validated milestones. We document, train your teams and hand over for autonomous operation.
Training and handover included: our leads document, explain and train your teams for autonomous operation. and project continuity with the same best practices.
Real questions
Wondering about something?
Direct answers about pharma, quality and compliance projects.
We track every action, version documents and produce structured compliance evidence.
Yes. Production data collection, report generation and electronic signatures according to your stack.
R&D projects, metadata, graph RAG, quality and sensitive process automation.
Integration in your approved IT, encryption, access rights and vulnerability scans.
We deliver a robust, tested and documented foundation. Production switchover happens with your teams and governance.
RESOURCES
Articles on Pharmaceutical & Health
Practical methods, feedback and sector insights.
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Ready to discuss your project? Book a 20-min strategy call
Tell us about your friction. We define your North Star, its metrics, and how to make your MVP measurable.