From small molecule to biologics to cell and gene therapy, drug development generates dense, regulated data that has to stay traceable. Uncountable structures discovery, formulation, and process data in one platform — with the audit trails and access controls regulated teams need
Design large scale multivariate experiments.
Automatically identify most promising candidates.
Use past data to suggest new experiments or identify critical variables.
Create complex workflows with an arbitrary number of steps
Request, assign, and track lab work.
Create & View Graphical reports
Monitor sample locations and results across multiple labs.
Track inputs across experiments by lot number.
Upload data through an automated process.
Uncountable helps you meet your compliance needs. With SOC 2 certification, plus ISO 27001, FDA 21 CFR Part 11, and GMP compliance, your most sensitive data stays secure.
Audit trail of all actions
Electronic signature support
Full lot traceability
Shelf life management
Inventory and workflow task management
Incorporate regulatory and pricing information from existing systems
Independently-verified best practices for storing and securing data
Built with secure cloud infrastructure on AWS
Permissions-based access means team members only see what they need to
Uncountable structures discovery, formulation, and process data across small molecule, biologics, and cell & gene therapy in one platform, with screening, DOE, and machine-learning-assisted experiment suggestions.
Uncountable centralizes assay, formulation, and process data in one searchable platform and uses correlation analysis and DOE to surface what drives results, so teams run fewer, better-targeted experiments and move from discovery to scale-up faster.
Yes. Uncountable tracks cell line genealogy across passages and transfections, models media optimization, and connects bioprocess scale-up conditions to outcomes like growth, stability, and purity.
