Enterprise R&D Software for Pharma & Biotech

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

Use cases

Design of experiments

Design large scale multivariate experiments.

High throughput screening

Automatically identify most promising candidates.

Predictive tools

Use past data to suggest new experiments or identify critical variables.

Multi-Step Processes

Create complex workflows with an arbitrary number of steps

Lab requests

Request, assign, and track lab work.

Reporting

Create & View Graphical reports

Sample tracking

Monitor sample locations and results across multiple labs.

Inventory management

Track inputs across experiments by lot number.

Automated data ingestion

Upload data through an automated process.

Research areas

Small Molecule

  • Discovery: Screening assays for cancer enzyme suppression
  • Aggregation: Compare synthesis pathway data for cost & efficiency
  • Formulations: Run correlation analysis on tablet formulations to identify the inputs that most affect dissolution and stability
  • Predictions: Use ML to suggest optimal formulations

Biologics

  • High throughput screening: Identify high performing cell cultures across large multiparametric experiments for directed evolution or engineered pathways
  • Cell line development: Easily track history of a cell line’s development cycles across passages
  • Media development: Use ML to project optimal media components
  • Bioprocess scale-up: Identify high growth, high stability operating conditions that generate high purity
  • Downstream processing: Compare separate efficiency across operating conditions
  • Molecular biology: Embed and view SnapGene files and incorporate plasmid constructs into experimental parameters.

Cell & Gene Therapy

  • Viral line development: Track genealogy across passages and transformations.
  • Cellular assay development: Evaluate binding effectiveness with target cells and proteins.
  • Molecular biology: Search qPCR data by the presence of engineered plasmid constructs.

Trusted by

St. Jude Children's Research Hospital
Beiersdorf
Lesaffre
Meggle
Global Health Labs

Compliance

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.

01

Audit trail of all actions

02

Electronic signature support

03

Full lot traceability

04

Shelf life management

05

Inventory and workflow task management

06

Incorporate regulatory and pricing information from existing systems

Security

Secure Data

Independently-verified best practices for storing and securing data

Cloud

Built with secure cloud infrastructure on AWS

Access Config

Permissions-based access means team members only see what they need to

SOC 2 certified

FAQs

How does Uncountable support pharma and biotech R&D?

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.

How does Uncountable speed up formulation and process development?

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.

Can it manage cell line and bioprocess data?

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.

See how Uncountable transforms research & development