Smart search across regulatory documents and SOPs
Ask in plain language about your SOPs, dossiers and applicable regulation and get the answer with the exact citation, document and version. Knowledge stops depending on who has been around longest.
Industries
AI and automation for Pharma & Biotech
In pharma and biotech, documentation is the work: regulatory, quality, scientific literature, pharmacovigilance. AI organizes it, summarizes it and makes it searchable, with the traceability a regulated environment demands.
Where it hurts
What's costing you time and money today.
- Huge, ever-changing regulatory documentation that must be known in detail
- Relevant scientific literature growing faster than anyone can read
- Quality records and deviations documented by hand, consuming hours of skilled staff
- Pharmacovigilance requiring review and classification of ever-growing volumes of notifications
What we build
Concrete solutions, not promises.
These are real automations we've built for this sector. Every project starts from your own processes, not a closed catalogue.
Scientific literature monitoring
The AI monitors publications and sources relevant to your molecules or therapeutic areas and delivers periodic summaries of what truly affects your work, with links to the originals.
Quality records and deviations
Documentation for controls, deviations and CAPAs is generated with AI assistance from process data, using validated templates and mandatory human review before signature.
Pharmacovigilance support
Suspected adverse reaction notifications are classified and prioritized automatically, with urgent cases escalated immediately. The team reviews and decides on pre-sorted material, not an unfiltered inbox.
Applicable services
How we make it happen.
We combine these services depending on what your case needs. In the free audit we tell you where to start.
Frequently asked questions
Common questions about this sector
Have another question? Write to us and we'll answer within 24 hours.
How does this fit a GxP environment?
We design every solution for regulated environments: the AI assists and a qualified person reviews and signs, with an audit trail for every step and traceability from every data point to its source. Together with your quality team we define which processes admit AI assistance and under which controls.
What about the confidentiality of research data?
Data never leaves a controlled environment with encryption and restricted access, and is never used to train public models. We sign whatever confidentiality agreements your legal department requires before seeing a single document.
We are a small biotech. Can we afford this?
The usual entry point is a contained one: for example, smart search over your documentation or literature monitoring. These are projects of weeks that free hours of very expensive profiles, and from there you scale if the numbers hold up.
Pharma & Biotech
Tell us about your processes and we'll tell you exactly what to automate.
In a 30-minute call we analyse your operation and hand you a report with the AI opportunities in your business. No strings attached.