One intelligence platform, from discovery to patient access.

HERMS connects evidence and decisions across advanced therapies, clinical development, manufacturing, regulatory affairs, market access, patient safety and compliance.

Regulatory operations

Turn regulatory complexity into decision intelligence. Connect regulatory requirements, submission evidence, scientific documentation and governance workflows. RULEXIS selects a defensible registration pathway. SYNCRA builds a consistent authority-ready dossier. REGAXIS keeps variations, renewals and commitments visible.

Patient safety operations

Anticipate risks. Protect patients. Transform disconnected safety signals and clinical evidence into actionable, traceable intelligence. AEVOX prepares safety reports for qualified case review. VIGILIX prioritizes emerging safety concerns for evaluation.

Manufacturing operations

From benchtop velocity to full-scale production. Accelerate tech transfer, optimize yield predictability, and engineer faultless manufacturing validation across every production line. INNEXIS, SYNTRIX and UNIFORGE support technology transfer, bioprocess and scale-up, and manufacturing consolidation.

Market access and evidence

VALTRIX tests whether evidence supports a payer value claim. VALTIRA compares defensible price and access scenarios. TENDRIX turns tender documents into a bid decision.

Governed AI you can audit

Purpose-built AI models for pharmaceuticals, med-tech and governments. Each model is architected for regulated, evidence-grade decision-making and trained on domain-specific regulatory, clinical, manufacturing and market data. The model proposes. The rules engine decides. The audit trail records both.

See all 25 HERMS solutions | Contact HERMS