Evarx Standard
Hosted general-purpose proprietary LLM for non-sensitive workflows.
- Strong general reasoning
- Pay-per-token pricing
- Hosted by Evarx · in-region
- Ideal for prototyping
Evarx is the medical AI platform for pharma and healthcare. Build private agents, fine-tune CPU-runnable medical SLMs on your own data, and deploy in your own infrastructure — in hours, not months.
Recognised by


One pipeline, three intelligence options. Every step is composable, audited, and deployable into the infrastructure you already trust.
Choose Standard, Private (Evarx Medical SLM), or Custom (rapid fine-tune).
EMRs, S3, SharePoint, PubMed, ClinicalTrials.gov, internal PDFs. Data both retrieves and refines.
Start from 10+ medical agent templates or compose your own with the drag-and-drop builder.
One click to API. Run on CPU on-prem, in your VPC, or as managed SaaS. Usage-metered billing.
Most customers start on Standard, move sensitive workloads to Private, and unlock durable advantage with a Custom fine-tune trained on their proprietary data.
Hosted general-purpose proprietary LLM for non-sensitive workflows.
Healthcare-trained small language model, deployable in your VPC.
Upload your data, get a custom-trained CPU-runnable model in hours.
Most platforms stop at retrieval. Evarx goes further — every interaction can refine a model you actually own. No vendor lock-in. No data leaving your perimeter.
CPU-runnable
Quantised SLMs deploy on existing servers — no GPU procurement.
Air-gapped ready
Ship in a Docker image to disconnected hospital networks.
Continuous refinement
Workflows feed validated outputs back into the next training cycle.
Hours, not months
Pre-built medical pipelines mean your first usable model lands the same day.
Custom SLM lifecycle
Upload data
PDFs, EMRs, datasets
Validate
PHI redaction, schema check
Fine-tune
GPU cluster, eval harness
Deploy
CPU on-prem or VPC
Continuous loop
Each completed workflow generates new supervised pairs. Schedule nightly refresh runs and your model improves while you sleep.
Protocol summarization, eligibility extraction, ICF Q&A across study sites.
ICSR triage, MedDRA coding suggestions, signal narrative drafting.
CSR sections, plain-language summaries, regulatory submission drafting.
CDSCO, FDA, EMA guidance retrieval grounded in your dossier history.
Daily PubMed digests filtered by therapeutic area, with extracted endpoints.
Real-time scientific Q&A grounded in your approved content library.
Pre-visit summarization and structured note drafting from unstructured records.
Marketing collateral pre-screen against approved labels and PI.
Built for regulated medical workloads.
Compliance is a feature, not an afterthought.
DPDP Act 2023
India data residency
HIPAA-aligned
PHI handling
On-prem & VPC
Air-gapped ready
RBAC + audit
Full trace logs
ISO 27001
In progress
A 30-minute call. We'll map your highest-leverage workflow, scope a fine-tune, and show you what runs in your VPC by next week.
No spam. Your message reaches a founder, not a CRM funnel.