The hard part isn’t the science.
It’s everything after it.
That’s why we built Tribal: one platform that carries an asset from the first search to a filed submission, so your budget goes into the molecule instead of the paperwork around it.
This is the
Tribal platform
One workspace, from search to submission
Your source data, your documents and your team sit in one place, where each step feeds the next. Search the asset universe, draft to eCTD structure, and check every claim against the file it came from, without moving between four tools to do it.
- Every claim traced to its source
- Built to eCTD from the first draft
- Gaps flagged before a reviewer finds them
- One audit trail across the whole programme
Ask in plain English or screen by field. Tribal reads public, licensed and internal sources together and returns a ranked shortlist with the evidence behind every score.
| Asset | Phase | Modality | Score |
|---|---|---|---|
| TB-2071 | Phase 2 | Small molecule | 94 |
| Ferristat | Phase 1 | Biologic | 88 |
| AV-118 | Preclinical | Small molecule | 81 |
Start from the eCTD module you need. Tribal assembles each section from your source files, fills the tables, and leaves a marker anywhere the data does not yet support the claim.
- 1 Administrative information Done
- 2.4 Nonclinical overview Done
- 2.6 Nonclinical written summaries Drafting
- 2.7 Clinical summary To do
- 3.2.P Drug product To do
Every statement carries the file, page and table it came from. Tribal checks each one back against the source and raises what a reviewer would raise.
No treatment-related findings were observed in clinical chemistry or histopathology at or below 120 mg/kg/day.28d_tox_study.pdf · p.14, Table 8
Gap: NOAEL not stated for the 28-day study
Draft in the
document editor
Say what you want changed
Ask for a change in a sentence. Tribal rewrites the affected passages in place and shows them as tracked edits, with the source for anything it adds. Nothing enters the dossier until you accept it.
- Edits arrive redlined, never silently applied
- Cross-references and tables update together
- Every insertion carries its source
Add the 10 mg/kg dose group and state the NOAEL for the 28-day study.
2.6.6 Toxicology written summary
Rats were administered 13F-SFA by oral gavage once daily for 28 days at dose levels of 0 (vehicle control), 10, 30 and 120 mg/kg/day.
No treatment-related findings were observed in clinical chemistry or
histopathology at or below 120 mg/kg/day.
The NOAEL could be calculated to be 150 mg/kg.
The NOAEL was 120 mg/kg/day, based on the absence of adverse findings at
this dose.
Source 28d_tox_study.pdf · p.14, Table 8
