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Healthcare & Pharma

Cut the documentation load so clinicians treat and teams ship, with compliance built in from the start.

Healthcare and pharma drown in documentation, and every line of it carries regulatory weight. geist takes the writing, coding and checking off your people's plates so clinicians spend time with patients and study teams spend time on the science.

Because it is compliant by design, runs in Germany, and keeps an audit trail on everything it touches, you get the productivity of AI without the exposure that usually comes with it.

What it does

Automated doctor's letters

Discharge summaries and referral letters are drafted from the record so clinicians review and sign instead of writing from scratch.

AI coding for billing

Diagnoses and procedures are mapped to the right codes automatically, reducing rejected claims and the rework they cause.

Trial and QC analysis

Study data and quality control results are read and summarized so deviations and signals surface early, with the source kept for review.

Compliance checks and audit trails

Documents are checked against your SOPs and regulatory rules, and every AI action is logged so an inspector can follow exactly what happened.

Clinical knowledge search

Staff query guidelines, formularies and internal protocols in plain language and get grounded, cited answers instead of guesswork.

In practice

A hospital department drafts discharge letters with geist straight from the patient record. The physician reviews and signs in a couple of minutes, documentation backlog shrinks, and the wording stays consistent across the team.

What you get

  • Hours of documentation returned to clinical staff each week
  • Fewer coding errors and rejected claims
  • Earlier detection of trial and QC issues
  • Audit trails on every step, ready for inspection
  • Consistent, compliant wording across the organization

Questions

Is patient data safe and compliant with GDPR?
Yes. geist is compliant by design and can run entirely on servers in Germany on your own infrastructure, so patient and study data never leaves your environment.
How does this fit the EU AI Act?
We assess each use case for EU AI Act obligations, including the higher bar that applies to health contexts, and build the documentation and human oversight those obligations require.
Will it replace clinical judgment?
No. geist drafts, codes and checks; clinicians review and decide. Every output is reviewable and traceable to its source.
Get started

Less paperwork, more care

Book a call and we will pilot one documentation or coding workflow with compliance built in.