Industries

Built for your role
in the pharmaceutical chain.

NASHRA understands that manufacturers, regulatory teams, medical affairs, and distributors have different needs. We've built for all of them.

01
Service 01
Full lifecycle ePI management

Pharmaceutical Manufacturers

NASHRA replaces your manual workflow end-to-end. From PDF ingestion to FHIR bundle submission.

See manufacturer features
Capabilities
  • Manual Word → XML conversion taking days
  • No version control across product portfolio
  • Fear of submission errors causing JFDA rejection
02
Service 02
Submission-ready, always

Regulatory Affairs Teams

Reduce submission turnaround time dramatically. Every output is audit-ready from day one.

See RA features
Capabilities
  • Submission turnaround measured in weeks, not hours
  • No single system connecting source docs to output
  • Defensible audit trail missing for inspections
03
Service 03
Portfolio visibility at scale

Medical Affairs / MAH

One dashboard for your entire MAH portfolio. Always compliant, always current.

See MAH features
Capabilities
  • No centralized view of current vs. outdated leaflets
  • Translation management is entirely manual
  • Distributing approved content to partners is chaotic
04
Service 04
Verified, always-current ePI

Distributors & Drugstores

Access always-current, manufacturer-approved ePI through NASHRA's Shared Dossier feature.

See distributor features
Capabilities
  • Receiving outdated leaflets from manufacturers
  • No way to verify if received content matches FHIR bundles
  • Compliance liability from outdated distributed content

Not sure which plan fits your role?

Book a 30-minute demo and we'll walk you through the exact features relevant to your workflow.