The inevitabilities
shaping life sciences
Data / model explosion
-omics, spatial biology, healthtech and sensor streams are compounding; specialized models proliferate
AI swarms become norms
General and specialized models, datasets, and tools must collaborate on shared tasks.
Infrastructure complexity
Enterprise deployments cross data silos, compliance firewalls, and regulatory constraints
Context is computational
System prompts, action prompts, data focus (RAG), and workflow design must be captured as a software layer available to models
Execution wins
Visual coding and the ability to nest workflows drives up design quality and engineering velocity.
Our thesis
What is Salt?
How it works
Transparent collaboration, powerful results
Key features
Track versioned runs and compare model outputs.
Hot-swap models while preserving workflows.
Enable non-coders to make live changes safely through drag-and-drop nodes with exposed parameters
Data is vectorized at the workflow level
Use cases
Compliant deployments
Deployment modes
Lightweight mode: A compact, all-in-one single-machine setup ideal for rapid prototyping, pilot studies, and development environments. It minimizes setup time so you can focus on breakthroughs.
Scalable mode: Multi-node architecture with separated core services and runners. It enables parallel processing to handle growing datasets and complex simulations without bottlenecks.
Enterprise mode: High-availability autoscaling on cloud infrastructure. It is designed for mission-critical biomedical applications that demand uninterrupted performance and reliability under heavy loads.
On-prem, VPC, or air-gapped deployment: Securely install behind your firewall. Leverage existing compute resources like GPUs, HPC clusters, or hybrid cloud setups—perfect for sensitive research environments requiring data sovereignty.
Compliance and trust
Fully SOC 2 and HIPAA compliant. It safeguards patient data and intellectual property with enterprise-grade security standards.
Built-in traceable retrieval, comprehensive audit trails, and support for 21 CFR Part 11-ready workflows. It ensures regulatory adherence for FDA-validated processes and fosters confidence in every step of your biomedical pipeline.