A tool for one job. Built in Basel. Shipped with an open spec.
Preclari is the AI-preflight layer: a tool for one specific question (is this workflow appropriate?) wherever an AI workflow enters a regulated process. Before the pilot, it lists the requirements that apply, the controls that are missing, and the questions a reviewer will ask.
The work that became Preclari started as a recurring deliverable inside a Basel-based advisory practice: a structured pre-deployment review of a pharma AI workflow, run before the pilot. Preclari is the productised version of that deliverable: sharpened, formalised, and shipped with an open specification so the artifacts it produces outlive the tool. v0.1 ships with the pharma GMP corpus; medtech (EU MDR + FDA) and the EU AI Act high-risk regime are next.
A workflow-first contract. Built for agents, audited by humans. Built in Basel, with a sister practice at practice.pramod.ch.
Pramod leads Preclari's strategy and product. He brings 25 years of pharma compliance and traceability infrastructure (track-and-trace, serialisation, computerised systems) at Pfizer, Gilead, AstraZeneca, BASF, and Novo Nordisk, and designed the Tatmeen national track-and-trace system for the UAE Ministry of Health. He also founded ChainAlign, decision intelligence for enterprise workflows and portfolios.
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Ani focuses on Preclari's regulatory accuracy: the evaluation sets and corpus ground-truth that decide whether a preflight check is correct. A PharmD candidate at UNC Eshelman School of Pharmacy, he built a global IND-requirements reference tool in a regulatory-strategy role at Roivant, and is a co-author on a 2025 Nature paper.
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Ankith works on Preclari's platform and hosted infrastructure. A computer-science student at Missouri S&T, he brings cloud and backend engineering (GCP, distributed messaging pipelines, CI/CD) from a software-engineering role at The Home Depot.
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Thomas contributes to Preclari's capital-side regulatory coverage: the corpus, the evaluation cases, and the design-partner feedback for facility builds, cleanroom and HVAC qualification, commissioning, and equipment IQ/OQ. He brings pharma engineering and project-management expertise from capital projects across Basel.
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Andrew contributes to Preclari's operations-side regulatory coverage: the corpus, the evaluation cases, and the design-partner feedback for ATMP and biologics GMP operations, tech transfer, and compliance auditing on running facilities. He brings operations-side GMP expertise as a manufacturing subject-matter expert.
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