What medical writing does Nora produce?

Nora translates complex clinical and scientific information into accurate, appropriately formatted content — regulatory submissions, clinical study reports, journal manuscripts, patient information materials, and healthcare professional communications.

How do I install Nora?

Download the .md file, paste the full contents into Claude Projects Instructions, specify the document type and audience, and start your medical writing session. Works with Claude, ChatGPT, or any AI chat.

Which AI tools does Nora work with?

Works with Claude (recommended), ChatGPT, and any AI chat accepting system prompts. Claude's long-context capability makes it the strongest choice for Nora's complex medical document writing workflow.

Does Nora follow specific regulatory guidelines for medical writing?

Yes. Nora applies ICH guidelines, EMA and FDA document requirements, CONSORT and PRISMA reporting standards, and Good Publication Practice — and flags which guidelines apply to the specific document type you are producing.

What is included in this download?

One .md skill file delivered instantly after purchase. All outputs are first drafts for qualified scientific review. Paste into Claude Projects Instructions and Nora is ready immediately. Works with Claude, ChatGPT, or any AI chat.

AI Medical Writer Skill for Claude & ChatGPT

Nora writes CSRs, SmPCs, journal manuscripts, HTA dossiers, and patient information leaflets inside Claude. Audience-calibrated. No fabricated data. Draft for review.

Nora — Medical Writer AI Skill

$29.00

Nora — Medical Writer AI Skill

$29.00

Digital download — instant access

Nothing ships. The moment checkout completes, your download link lands in your inbox. Pay once, keep forever — no subscription, no expiry. Works with Claude, ChatGPT, and any AI chat. Secure checkout handled by Shopify.

30-day money-back guarantee. If it doesn't perform as described, email us and we'll issue a full refund — no questions asked. Refund policy

Drop Nora into Claude and get a Senior Medical Writer who translates complex clinical and scientific information into accurate, appropriately formatted content — regulatory submissions, journal manuscripts, clinical trial documentation, HTA dossiers, patient information leaflets, CME materials, and plain language summaries across every medical writing format.

The same clinical trial data requires completely different writing for an EMA regulatory summary, a journal article, a conference abstract, a GP reference guide, and a patient leaflet. Nora is one of the most audience-calibrated AI medical writing tools available in Claude format — built for pharmaceutical companies, CROs, medical communications agencies, and freelance medical writers. She asks for target audience and document type before producing anything, never fabricates clinical data (missing values are [DATA TO BE PROVIDED] placeholders), and flags regulatory compliance requirements — while noting that final regulatory sign-off requires qualified regulatory affairs review.

What you get

→ Regulatory writing — Clinical Study Report (CSR) sections and narratives, Summary of Product Characteristics (SmPC) drafts, Patient Information Leaflet (PIL) and Instructions for Use (IFU), Investigator Brochure narratives, Risk Management Plan (RMP) narrative sections, and Common Technical Document (CTD) summaries meeting ICH E3, EMA, and FDA requirements
→ Clinical trial documentation — study protocol and protocol synopsis drafts, Statistical Analysis Plan (SAP) narrative sections, Informed Consent Form (ICF) drafts structured to Declaration of Helsinki and ICH E6 GCP standards, Case Report Form (CRF) completion guidelines, and DSMB/IDMC charter sections
→ Publications and scientific communications — journal manuscript sections (introduction, methods, discussion) following CONSORT, PRISMA, and STROBE reporting standards, conference abstract drafts, systematic review and meta-analysis narrative sections, literature review sections, and responses to peer reviewer comments
→ Patient-facing materials and plain language summaries — plain language summaries of clinical trials for non-specialist audiences, disease awareness patient content, patient support programme materials, lay summaries of research, and patient information materials written to health literacy standards with GPP3 compliance awareness
→ Medical education materials — Continuing Medical Education (CME) content, slide deck scientific narrative, symposium and advisory board materials, disease awareness materials for HCPs, prescribing guide narratives, and healthcare professional training materials following ABPI Code of Practice (UK) standards
→ Health technology assessment and outcomes — NICE and SMC HTA dossier narrative sections, value dossier summaries, real-world evidence summaries, budget impact model narratives, and health economics evidence synthesis structured to meet HTA body submission requirements

📄 nora-medical-writer.md

Under 2 min install

Works with Claude Sonnet 4 & Claude Cowork

How to install

Download the .md file → open Claude → paste the file content into your system prompt or Project instructions → provide the document type, target audience, and clinical data or context → Nora produces scientifically accurate draft content instantly. All outputs are first drafts for qualified scientific or medical team review before submission or publication.

How to install Under 2 minutes

Four steps. Any AI chat.

01
Download the file
After checkout, the download link lands in your inbox. Save the file anywhere on your device.
02
Open your AI chat
Claude, ChatGPT, Gemini, Grok, or Copilot — whichever one you already use.
03
Paste the file contents
Drop it into the system prompt, Project instructions, or custom instructions field.
04
Start working
Your AI is now configured as a specialist. Ask it anything inside its domain.