PROFESSIONS

Agents for pharma & life sciences

Documents, quality and scientific knowledge, under GxP, traceability and sovereignty.

01 / What guides our engagements

GxP
Regulated validation
SCOPE
Data inside the agreed frame
HITL
Human in the loop
Evidence
Outcomes defined before deployment

02 / The problem

Pains we know too well

  1. Regulatory document volumes

    Reviews and synthesis too slow for timelines.

  2. Scattered scientific knowledge

    Papers, SOPs, trials: signal hard to retrieve.

  3. GxP / audit requirements

    No opaque automation in a regulated environment.

03 / The solution

What Remparia can build for you

  • Document assistants with audit trail
  • Governed scientific / SOP RAG
  • Quality / deviation agents with validation
  • Audit-compatible architecture and governance
  • Documentation, training and transfer of ownership to your teams

04 / Business agents

What the agent carries, and what it never touches

Illustrative

Intervention prepared

Prepare maintenance / quality / exception files for field teams.

Trigger
Alert, non-conformity, shift, SLA.
Inputs
Procedures, history, tickets.
Tools
MES / ERP · DMS · Ticketing
Deliverable
Intervention file + points to validate.
Human validation
Diagnosis, safety, stop decision.
Never does
It does not stop a line or certify compliance.
We measure
Prep time before intervention.

05 / Use cases

Three concrete use cases

Illustrative scenarios. Every deployment is scoped with signed KPIs before production.

Medical / regulatory
Need

Target to define : Speed document reviews.

Remparia

Possible deployment : Pre-analysis pipeline + checklist, human sign-off.

Quality
Need

Target to define : Reuse SOPs and deviations more effectively.

Remparia

Possible deployment : RAG + investigation assistant, full traceability.

Regulatory affairs
Need

Target to define : Consolidate regulatory watch without drowning teams in PDFs.

Remparia

Possible deployment : Watch agent on approved corpora: dated summaries, source links and major-change alerts.

07 / FAQ

Frequently asked questions

GxP compatible?

We design with your validation / audit requirements, with no shortcuts.

Clinical data?

Minimization, rights and hosting framed with your compliance teams.

Do we remain autonomous after deployment?

Yes. GxP SOPs, audit trails and e-signature rules are documented; regulatory validation stays internal.

// READY TO START

Show us the workflow costing you time.

In one hour, we frame repetitive work, data constraints and the gains to measure. With a partner, not a salesperson.