NEUVIOR is a UK healthtech company building PHARMORIS, a staff-facing medicines action, evidence and governance platform.
PHARMORIS is designed to help healthcare organisations move from medicines signals into governed action: ActionCases, evidence packs, human review, source traceability, blocker tracking, stakeholder acknowledgement, value review and audit trails.
The product is not an autonomous prescribing tool, not a prescribing engine and not a replacement for pharmacists, clinicians, finance, procurement or governance. The current focus is controlled pilot-readiness: credible evidence, clear intended use, source provenance, clinical-safety awareness, information governance, accessibility, standards alignment and decision-grade reporting.
NEUVIOR is especially interested in meeting people working on regulatory science, standards, NHS innovation, AI assurance, clinical safety, medicines optimisation, medtech commercialisation, evidence generation and public-interest innovation.
We are looking for practical conversations with people who can help pressure-test how a health software product moves safely from prototype evidence to controlled pilot use: what evidence matters, what buyers trust, what risks must be controlled, and what makes innovation credible enough to adopt.