Cell Technologies — AI-native pharmaceutical R&D

One connected workflow

Every stage feeds the next — the way real drug development actually flows.

◇

Discover

Targets, candidates, modality

Oracle

⬡

Design the trial

Endpoints, eligibility, sample size

Delfi

◎

Build manufacturing

Process, QC, CMC

Oracle

◈

Prepare the filing

IND / regulatory documents

Delfi

Two products, one platform

Intelligence and execution, working together.

Oracle finds and shapes the science. Delfi turns it into a trial and a filing. What you build in one flows straight into the other.

Oracle

Therapeutic & manufacturing intelligence

Go from a disease or a compound to a full development picture — candidates, mechanism, modality analysis, quality control, and a manufacturing process — in one pass.

✓ Discover druggable targets and candidate therapies
✓ Analyze modality, mechanism, and competitive landscape
✓ Design manufacturing and QC, grounded in your modality

Oracle · Modality analysis

◇

Candidate discovery

Targets · antibodies · small molecules

Ready

◎

QC & specifications

Release criteria · stability · potency

Ready

⚙

Manufacturing process

Modality-specific CMC

Ready

Delfi · Trial builder

◈

Asset & program

Compound · indication · positioning

⬡

Endpoints & eligibility

Anchored to real guidance & trials

◆

Regulatory filing

IND-ready documents

Delfi

Clinical trial & regulatory builder

Define your asset, attach your evidence, and build a complete clinical trial — synopsis, design, endpoints, eligibility, and sample size — then assemble the regulatory filing.

✓ Design the trial from a structured program dossier
✓ Endpoints and eligibility grounded in real ClinicalTrials.gov and literature evidence
✓ Assemble IND-ready regulatory documents

Why teams choose Cell Technologies

The work of a full R&D team, at the speed of a conversation.

⚡Hours, not months

Compress work that takes teams weeks into a single working session.

◈A fraction of the cost

Replace fragmented consultants and tools with one integrated platform.

✓Grounded in evidence

Outputs are anchored to real trials, literature, and regulatory guidance — not guesswork.

◆Regulatory-ready

Produce structured, submission-shaped documents you can take forward.

Build your clinical trial and regulatory files in hours, not months — and at a fraction of the cost.

Oracle

Delfi

Discover

Design the trial

Build manufacturing

Prepare the filing

Intelligence and execution, working together.

Oracle

Delfi

The work of a full R&D team, at the speed of a conversation.

Build your first program today.