Marketing built to clear regulatory review.
Marketing built for regulated claims and long evaluation cycles, read by clinicians, procurement and distributors.
Talk with an O8 specialist
Tell us what you need help with. We'll scope it with you.
What we produce for device marketers.
Built around the specifier, the committee, and the regulatory line.
Indication demand research
How clinicians and specifiers search for the problem your device solves — by procedure, mechanism, and setting.
On demandCompetitor claim analysis
What competitors claim, how they support it, and where your evidence lets you say something stronger.
On demandEvidence-linked content drafts
Technical content drafted with sources attached and structured for regulatory review rather than rewritten after it.
Included with your engagementStakeholder-specific messaging
Clinician, procurement, biomed, and distributor messaging separated so one page is not asked to do four jobs.
Included with your engagementDistributor & channel enablement
Channel-ready materials kept consistent with the approved claim set, so partners are not inventing language.
Done for youTechnical AI visibility
Whether AI assistants cite your device for its indication — and what structural gaps prevent it.
On demandIndication demand
How clinicians actually search for the problem you solve
Review status: Mapped.
Example output: Indication & competitor claim map.
Connection status: Regulatory review required.
Example request: “How are competitors positioning against our indication — and what can we legally say back?”
Context: Your evidence base · Clinical review · Regulatory sign-off.
Competitor claims
What rivals assert, and where the evidence gap sits
Review status: Compared.
Claim review gate
Every claim routed to regulatory before publish
Review status: Enforced.
Each item is labeled by how you get it. On demand — bought as a single defined deliverable. Included with your engagement — already covered if we run your marketing. Done for you — we build it and operate it.
Limits your regulatory reviewer can hold us to.
Start with one deliverable. Expand after your reviewer signs off.
Buy one defined deliverable
One scoped audit or brief, delivered and reviewed.
Try it freeAdd it to your existing engagement
Grounded in your analytics, your content, and the campaigns you are already running.
Book a scoping callBuilt and operated for you
Connections designed, tested, documented, and run — or handed to your team.
AI employee setupNot sure which fits? Start with one small project and judge the output.
Book a scoping callThe wider healthcare picture.
All healthcare segments
Provider systems, B2B healthcare and payers, life sciences, and the shared compliance guardrails.
See all healthcare segmentsData & integrations
Which systems connect, what stays read-only, and how approvals work before anything is written.
See data connectionsHow the product works
The three access paths, what automation does, and what a specialist always owns.
See how it worksFast turnaround. Same claim standard.
Automation handles retrieval, competitor comparison, and drafting. Specialists own claim accuracy and positioning — and your regulatory reviewer keeps the last word.
See client outcomesBring one indication. Review the draft yourself.
Bring a live question. You get a scoped deliverable a specialist has reviewed — not a demo.
