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ICDMO CDMO
Full-Service CDMO

From AI Design
to GMP Delivery

ICDMO integrates computational drug discovery with full-scale biologics manufacturing — a single partner for your entire development pipeline.

40+
Countries Served
19+
Years Experience
500+
Drug Targets
cGMP
Certified Facilities
End-to-End Pipeline

From Idea to IND — One Partner

Full Integration · Single Partner · Zero Handoffs
Molecular Modeling
Molecular Modeling
Research & Development
Research & Development
Bioprocess Manufacturing
Bioprocess Manufacturing
Analytical Testing
Analytical Testing
Why ICDMO

Built for Speed. Designed for Scale.

10×
faster lead ID
AI-Accelerated Discovery
AlphaFold2, molecular dynamics, and proprietary ensemble models compress target-to-lead timelines from years to weeks.
500+
validated targets
Full Biologics Portfolio
Stable cell lines, recombinant proteins, antibodies, ADCs, and viral vectors — all under one roof.
ISO/ICH
compliant
GMP-Ready Infrastructure
cGMP-certified suites for plasmid, viral vector, protein, and antibody manufacturing with full regulatory documentation.
19+
years experience
End-to-End Integration
Computational design and wet-lab execution on a single platform — zero vendor handoffs, zero data loss.
Therapeutic Modalities

We Cover Every Major Modality

🧬
Gene Therapy
AAV, Lentiviral, Adenoviral vectors — IND-enabling to GMP scale
⚗️
mRNA Therapeutics
Sequence design, LNP formulation, GMP-grade synthesis
🔬
Antibody & ADC
mAb, bispecific, VHH, ADC — from discovery to GMP batch release
🧫
Cell Therapy
Cell line engineering, viral transduction, cGMP cell banking
🔩
Protein & Enzyme
Recombinant expression, AI-optimized enzyme engineering & characterization
💊
Small Molecule
Target-based screening, drug profiling, structural biology support
Platform Overview

One Integrated Platform

iCDMO
Platform
AI & Compute
Bioinformatics
Wet Lab
GMP Mfg
QC & QA
Target ID
Lead Opt.
Pre-clinical
IND Filing
Phase I
Scale-up
CMC
GMP Batch
1
Compute → Bench Integration
AI predictions feed directly into wet-lab protocols. No re-interpretation, no data loss at the handoff.
2
Modular Engagement
Engage for a single stage or the full pipeline. Teams adapt to your project scope and timeline.
3
Regulatory-Ready Documentation
Every stage produces IND-compatible data packages. CMC documentation prepared in parallel with manufacturing.
4
Transparent Project Tracking
Dedicated project manager, regular milestone reports, and shared data portal for real-time progress.

Ready to Start Your Program?

Tell us where you are in your pipeline. We'll map the right entry point and put together a proposal within 48 hours.

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