Features
Multi-agent clinical trial design
Protocol outline generation
Patient enrollment forecasting
Endpoint selection rationale
Regulatory compliance checklists (FDA, EMA, ICH)
Literature search and evidence synthesis
Feasibility assessment reports
Export to Word, PDF, and CDISC SDTM format
Adaptive trial design templates (Bayesian dose-finding)
Rare disease agent workflows with natural history comparisons
Custom agent building via no-code editor
API access for enterprise integrations (Professional plan)
Version control and audit trail
Real-time collaboration for design teams
Therapeutic area-specific templates (oncology, neurology, rare diseases)
Quantum mechanics (QM) with Jaguar
Free energy perturbation (FEP+) for binding affinity
Molecular dynamics (MD) with Desmond
Docking and virtual screening with Glide
AI-driven retrosynthesis planning (RetroSynth)
Predictive Toxicology SAR panel for early liability screening
AutoDesigner for ultra-large chemical space exploration
Generative AI for molecular materials design
Nanoreactor with reaction barrier predictions
Structure prediction and target enablement
Antibody design and peptide discovery
Enzyme engineering and bifunctional degrader design
Biologics modeling with BioLuminate
Collaborative LiveDesign platform
Python API for workflow automation
