Knowledgeable
For clinical-stage CEOs & CCOs

Go into your next round with the value story your acquirer will use.

You don't have a 30-person Market Access function. You have one or two brilliant people, and a board that expects answers a Big Pharma team would need a quarter to assemble. Knowledgeable gives that lean team the capability of a department, from preclinical positioning to launch, so every Series C, business development conversation and partner meeting opens with the asset narrative your buyers will adopt verbatim.

0×
department-level capability
0%
less time on literature
0
outside vendors needed
Compounding evidence across the pipeline
42
Preclinical
indications scoped
18
Phase II
competing treatment studies
9
Phase III
endpoints validated
3
Launch
value stories live
Evidence Collection
FIH-stage asset · competitive landscape
0
Identified
0
Screened
0
Included
PRISMA-tracked · dual-reviewer · audit-ready
Ask Knowledgeable · Plan

"Plan a 12-week pre-launch value-story programme for our Phase 2 NASH asset."

Framing the objective
Mapping unknowns
Sequencing workstreams
Producing the plan document
ScopeWorkstreamsOwnersMilestones
5 workstreams · 18 milestones · 0 deliverables started
Chat-driven · or do it manually. Your call
Day-one wins

The results show up before the next board meeting.

Task
Before
With Knowledgeable
Literature search & screen
3 weeks
2 days10×
HTA precedent scan (EU5)
5 days
1 hour40×
Value story draft
2 weeks
3 days
Payer Q&A prep
4 days
1 day
From preclinical to launch

One system across the whole asset life.

No tool sprawl, no re-learning. The work your team did at Phase 1 powers the dossier you file at launch and the diligence pack your acquirer opens at term sheet. The same evidence base. The same audit trail.

Stage 01One MD-level lead can own this end-to-end

Preclinical positioning your board can defend

Indication scoping, competitive landscape and TPP drafting. Before you spend a million on a Phase 1 competing treatment your CMO will regret picking.

Stage 02Your CMO and CCO finally working off the same source of truth

Clinical strategy anchored to payer reality

Endpoint selection grounded in HTA precedent. Competing treatment choice anchored to what reimbursement bodies have actually accepted. Trial design that anticipates the AMNOG and NICE conversation, not retrofits to it after readout.

Stage 03The artefacts your acquirer will reuse on day one

Launch, business development and diligence, from one evidence base

Value story, payer dossier, HTA submission, pricing corridor and the data room your acquirer's bankers will tear through. All generated from the same evidence, all kept live as the data lands.

Compounding advantage

Your asset story never goes stale between rounds.

As trials read out, real-world evidence accumulates and competitors move, Knowledgeable keeps your value story, TPP and HTA positioning continuously current. No scramble to rebuild the deck the weekend before the board call, the business development pitch or the diligence room opens.

Lean by design

No standing army of consultants on the cap table.

Investor-grade

Every claim source-linked, every number defensible.

Preclinical
Clinical
Evidence
Launch
Compounds

Bring department-grade output to your next milestone.

Go into your next round prepared
FAQ

Frequently asked questions.

Yes, it's built for lean teams. One MD- or CCO-level lead can own indication scoping, TPP drafting, competing treatment selection and value-story work end-to-end, with the output a department would produce at a Top-20 pharma.
Responsible AI · Enterprise security

Diligence-ready without the enterprise drag.

SSO, mandatory 2-factor, full audit trail and EU/UK data residency on every plan. Move at biotech speed without giving your lead investor or your future acquirer's diligence team a reason to pause the conversation.

Manual or chat, your callEU AI Act alignedSSO + MFA enforcedAES-256 + TLS 1.2+EU / UK data residencyFull audit trail