Pharma & biotech

Pharma.
GLP and
21 CFR Part 11.

Eldric ships dedicated scientific tools for drug discovery and bench science. Molecular-docking pipelines, ADMET prediction, AlphaFold integration, LIMS with sample tracking and audit. The science worker has GLP and FDA 21 CFR Part 11 compliance modes built in.

Talk to us All use cases
Workloads

What people in this sector typically run.

Molecular docking

AutoDock / Vina / RDKit pipelines orchestrated through the science worker. Results stored against the project in matrix memory.

ADMET prediction

Pre-trained ADMET models with the option to fine-tune on your proprietary screening data. Your compounds, your weights.

AlphaFold integration

Local or cluster-hosted AlphaFold runs through the science worker. Structures cached and indexed.

LIMS with audit

Sample tracking, experiment management, hash-chained audit. GLP / 21 CFR Part 11 modes flip a regulatory-grade audit trail on.

Bench-to-paper

Pull from internal lab notebooks; cross-reference PubMed; draft methods sections. Citations preserved through the chain.

Per-program tenants

Different drug programs walled off from each other. Compulsory in pharma; default in Eldric.

Compliance & isolation

What we explicitly support.

GLP compliance mode FDA 21 CFR Part 11 e-records (Enterprise tier) EU GMP documentation-friendly GDPR Audit ledger hash-chained

Honest scope.

Eldric supports the scientific workflow; it does not replace the medicinal chemist, the regulatory writer, or the trial statistician. Every AI suggestion is reviewed by a qualified human before it informs a decision.

Next step.

Write to office@eldric.ai. Tell us what you are trying to do; we will tell you whether Eldric is a fit and, if not, what would be.