One system for a development program, from the first idea to the data room.
Most small pharma teams run a program across spreadsheets, shared drives, a project tool and three consultants. The Graticus Platform puts the science, the strategy, the regulatory path, the money and the deal in one place, with role-based access and a full audit trail on every change.
Its best-known part is the Protocol Generator. Give it a compound name, an image of the structure, or draw it; nothing generates until you confirm the structure is the one you meant. It then pulls the evidence from PubChem, ChEMBL, Europe PMC, ClinicalTrials.gov and EPO patent records, and writes a nine-section development brief, with every claim cited, that you can put in front of a partner.
Science and evidence
- Protocol Generator: a cited development brief in under three minutes, delivered as a versioned Word document with its citation register. A section that cites something ungrounded is regenerated once, then failed rather than shipped.
- A development plan that is not written by a model. It comes from a regulatory rules engine and a critical-path scheduler, and converts into a real project: a typical small-molecule program to IND/CTA-ready lands at roughly 30 milestones and 230 tasks across 252 days.
- Literature assistant, data interpreter and hypothesis generator, alongside your compound profiles and formulation records
Strategy and valuation
- Idea Explorer: start from an idea, get three to five options, each checked against public registers
- Compound screening and evaluation, regulatory gap analysis and prior-art research
- Opportunity, licensing and launch analysis, and a valuation of each program you can save and compare
Running the program
- Each program as a venture with milestones, tasks, approvals and time tracking
- Budgets, expenses, invoices and reconciliation, with vendor management
- Grant applications drafted from the program record
Regulatory, IP and deals
- Regulatory compliance, reports and a log of every agency interaction, for FDA 505(b)(2), ANDA and EMA pathways
- IP and patent portfolio, and patent work from invention disclosure through PCT
- Contracts, contacts and meetings, and a licensing data room with NDAs, analytics and a partner portal
On your data
- It never touches our pharma business. The Protocol Generator does go to public chemistry, literature and patent databases, and to the model that writes the prose. Every customer runs on their own deployment, and we put the data handling in writing before you upload anything.
- A support tool, not the last word. Your scientist, your regulatory lead and your patent attorney still decide.
Pricing
- Full platform — from $3,500/month
- Every module: the Protocol Generator plus strategy and valuation, program management, finance, regulatory, IP and the licensing data room.
- Protocol Generator access — from $1,750/month
- Billed annually. Dedicated instance, up to 24 briefs a year, project-plan conversion included.
- Single development brief — $3,500
- One compound, the complete document and register. Credited in full against either subscription if you continue.