AI Consultant in Basel

Basel is where global pharma lives. Roche, Novartis, and hundreds of specialized life sciences companies operate under some of the strictest documentation requirements in any industry. I build AI agents and RAG systems that work within FDA, EMA, and GxP frameworks. Clinical documentation, regulatory submissions, pharmacovigilance records. All searchable, all traceable, all compliant.

AI in pharma: Documentation is the product

In pharmaceutical companies, documentation is not overhead. It is the product. A drug cannot move forward without complete, accurate, and retrievable documentation at every stage. Clinical trial records alone generate thousands of pages per study. Regulatory submissions span multiple agencies and jurisdictions. Quality management systems require instant access to SOPs and deviation reports. RAG systems make all of this searchable with full source attribution. AI agents automate the classification and routing of incoming regulatory correspondence. The compliance requirements are strict. The technology can meet them now.