The AI first draft, done right —
so your writer can finish faster.

AcuityMedical does the heavy legwork with AI, handing your team a structured first draft of medical information content or PharmD continuing-education material. Your medical writer finishes and submits — or ours can, on request. Live now for PharmD CE; AI-leveraged medical information content coming soon.

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Where AI speed meets human rigor.

AI handles the heavy first pass. Your medical writer makes it submission-ready.

Coming Soon

AI-Leveraged Medical Information Content

First-draft medical information for pre-approval and post-approval products — we do the AI legwork, your writer finishes.

We're building an AI-leveraged drafting service for medical information content covering both pre-approval (investigational) products and post-approval (marketed) products. We do most of the legwork with AI and hand off a structured first draft; your medical writer finishes and takes it through MLR. No in-house writer? Ours can finish on request.

  • Product FAQ & SRL topic development — pre-approval and post-approval products
  • Literature searches and evidence summaries
  • First-draft Standard Response & Custom-Response Documents (SRDs/SRLs)
  • Hybrid AI: a local model drafts your confidential data-on-file; a frontier cloud model drafts the public sections
  • Optional medical-writer finishing available on request
Available Now

AI-Leveraged PharmD Continuing Education Support

An AI first draft of your CE — you finish, you submit, you get published.

We generate the AI draft; the pharmacist author (or their medical writer) finishes the manuscript and submits it for accreditation and publication.

  • Topic Suggester — surfaces timely, gap-driven CE topics
  • Proposal Drafter — ACPE-aligned proposals with measurable learning objectives, built for accreditation-readiness
  • Manuscript Draft — a full first-draft CE manuscript and post-test, ready for you to finish
  • You stay the author — you complete, review, and submit the final work for accreditation

We do the legwork. Your writer does the final mile.

AcuityMedical takes the slow part off your plate — the structured AI first draft — so your medical writer starts from a strong, sourced foundation instead of a blank page. They finish it through MLR and own the final output. Don't have a writer? Ours can finish on request. Either way, the heavy lifting is already done — and contract and independent medical writers use AcuityMedical the same way, to accelerate their own process.

Confidential content stays on your side. Public content moves fast.

The forthcoming medical information service is built on a deliberate split between confidential and public information — so speed never comes at the cost of control.

Your data-on-file stays local

Confidential, proprietary content is drafted by a local model on a private machine — never sent to any cloud AI.

Public sections use frontier AI

Open-access and published information is drafted with a best-in-class cloud model for speed and quality.

Separated by design

The architecture itself keeps confidential and public content apart — not policy alone, but how the system is built.

You own the output

Your medical writer — or ours — finishes the work and takes it through MLR. Accountability stays human.

Described for the forthcoming AI-leveraged medical information content offering.

Four steps, no friction.

Every engagement begins with a conversation, not an intake gauntlet.

01

Scope

Tell us the products, topics, and formats. We confirm fit and scope directly.

02

AI First Draft

We draft it — confidential data-on-file on the local model, public sections on the frontier cloud model.

03

You Finish

Your medical writer takes it through MLR — or ours finishes on request.

04

Delivery

A structured first draft (or finished piece) in your templates, ready to submit.

Built for the people who own the content.

From medical-information teams to individual CE authors — anywhere a strong first draft saves real time.

Pharma & Biotech Medical Information Teams

First-draft SRD/SRL volume for pre-approval and post-approval products.

PharmD CE Authors

Pharmacists who want to publish accredited CE without starting from a blank page.

Contract & Independent Medical Writers

Accelerate your own drafting — we do the first pass, you finish faster.

MI Vendors, CROs & Med Comms Agencies

Add AI-assisted first-draft capacity without new headcount.

Start a conversation.

Tell us what you're working on. We'll respond within one business day to discuss fit and next steps.

Based in
United States  ·  Remote engagements

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We'll reply to your email. You can also reach us directly at consulting@emersonarc.com.