Enterprise knowledge governance
Manage knowledge at individual, department, and organization levels, with knowledge graphs and hybrid retrieval providing a shared knowledge foundation for business agents.
Biopharmaceutical
R&D Agents
ChatDD - Insight
Knowledge insights and specialist reports for R&D and business decisions
Built on ChatDD 2.0’s industry knowledge base, specialist models, and multi-agent capabilities, Insight brings authoritative industry data and enterprise knowledge into a governed knowledge system. It automatically plans research workflows for program evaluation, competitive analysis, patent strategy, and BD decisions, producing structured reports and visual dashboards.
Global biopharma insights
Search and analyze pipelines, drugs, targets, molecules, literature, conferences, clinical data, and patents across multiple dimensions.
Specialist reports and BD decisions
Access 15 specialist report scenarios covering pipeline insights, global pharmaceutical company research, unmet clinical needs, and BD transaction decisions.
Patent insights and drafting
Support preliminary freedom-to-operate (FTO) risk screening, claim analysis, patent family geographic coverage, and expiry alerts, with multi-agent assistance for patent drafting.
ChatDD - Discovery
Natural language for early drug discovery and antibody design
Bring specialist knowledge, AI agents, and computational tools into a single workflow for early drug discovery and preclinical research. Researchers can use natural language to investigate research questions, generate candidate antibody sequences, and combine macromolecular docking with binding affinity predictions to guide iterative molecular design.
R&D through natural language
Describe research objectives in natural language and invoke specialist agents and algorithms for multimodal biomedical analysis.
Insights for early R&D
Use specialist Skills, industry knowledge, and the agent platform to investigate targets, drugs, pipelines, and relevant literature.
Antibody design and sequence generation
Generate candidate antibody sequences based on antigen and epitope information to support antibody discovery and iterative design.
Macromolecular docking and affinity prediction
Access macromolecular docking results and binding affinity predictions to help analyze interactions such as van der Waals forces, hydrogen bonds, and hydrophobic interactions.
ChatDD - Trial
Professional writing workflows for clinical research and regulatory documentation
Support more than 20 specialist scenarios across study start-up, safety, clinical study reports, and regulatory documentation. Parse uploaded materials, organize evidence, and generate drafts, then check, edit, preview, and export in one workspace. Missing or conflicting information is explicitly flagged for confirmation, and qualified professionals perform the final review.
Clinical writing workspace
Parse study materials and assist with drafting trial protocols and other clinical documents, with online editing, preview, and export in the same workspace.
CSRs and CTD 2.7 clinical summaries
Structure CSR drafts around study design and actual results, cross-check numerical content against tables, figures, and listings (TFLs), and integrate evidence for CTD 2.7 clinical summaries.
SAE / ICSR pharmacovigilance documentation
Organize patient information, suspect drugs, adverse events, and draft case narratives from source records, with final review by pharmacovigilance professionals.
Regulatory documents and specialist translation
Assist with product labeling drafts for regional requirements such as those of the NMPA and EMA, literature summaries, and specialist medical translation, grounding key facts in source materials.
AI + Experts Jointly SolveCore Challenges in Drug Discovery
Target Identification
- Disease analysis and clinical need insights
- Analysis of diseases and signaling pathways, development progress of investigational molecules, and the competitive landscape
Expert guidance
Experts assess target characteristics, clinical needs, competition & market opportunities to refine selection strategy
Program Initiation
- Identify and analyze unmet clinical needs
- Market assessment & competitive landscape
- Technical feasibility assessment
- Policy & regulatory monitoring and interpretation
Expert guidance
Experts recommend projects with growth potential based on the company’s strategy and strengths
New Molecule Screening
- Generate a library of candidate molecules
- Predict drug-likeness
- Cardiotoxicity prediction
Expert guidance
Experts assess the potential of candidate molecules and optimize synthesis routes and efficacy validation
Clinical Services & Regulatory Filing
- Clinical development plan (CDP) drafting
- Clinical trial protocol design
- Adverse-event prediction
- Patient recruitment:
Expert guidance
Experts combine AI results to recommend indications, dose-escalation strategies, and inclusion and exclusion criteria
Modernization of Traditional Chinese Medicine
- Mechanism-of-action research for traditional Chinese medicine (formulation–disease pathway analysis)
- Screening & optimization of new TCM formulas
- TCM package insert drafting
Expert guidance
Experts evaluate mechanisms of action and identify distinctive benefits
Enterprise-grade Security
Safeguard your company’s data and comply with the latest security standards