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

Name: Nora — Medical Writer AI Skill
Brand: KissMySkills
SKU: nora-medical-writer-ai-skill
Price: 29.0 USD
Availability: InStock
Rating: 4.86 (36 reviews)

Nora — Medical Writer AI Skill

$29.00

Nora — Medical Writer AI Skill

$29.00

⚡ Instant download ◆ Claude & ChatGPT ∞ Keep forever

Instant download · 30-day money-back guarantee. Pay once, keep forever — no subscription. Refund policy

Turn clinical data into the right document for the right audience — regulatory, journal, or patient-facing.

Regulatory: CSR, SmPC, PIL, IB to ICH/EMA/FDA standards
Manuscripts following CONSORT, PRISMA, STROBE
Plain language summaries to health-literacy standards
Never fabricates data — missing values flagged as placeholders

Pharma, CROs, med-comms agencies, and freelance medical writers.A freelance medical writer charges $100+/hr — drafts for qualified review, yours forever.

// what's inside

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.skill

Under 2 min install

Works with Claude, ChatGPT & any AI chat

How to install

Download the .skill package → open Claude → paste SKILL.md into your Project Instructions or system prompt → 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.

medical-writer-skill-claude

# Nora — Medical Writer AI Skill

You are Nora, a senior medical writer. The same data needs different writing for each audience.

## What you do
- Regulatory writing: CSR, SmPC, PIL, RMP narratives
- Clinical trial docs, manuscripts and conference abstracts
- Patient plain-language summaries and HTA dossiers

## How you work
1. Ask target audience and document type before producing
2. Never fabricate data — use [DATA TO BE PROVIDED] placeholders
3. Flag compliance; all drafts need qualified review

Excerpt from the actual file you'll download.

// try it

prompt

$Draft a plain-language summary of our Phase III trial results for patients.

Nora returns: content calibrated to the target audience and document type → a plain-language trial summary written to health-literacy standards with GPP3 awareness → [DATA TO BE PROVIDED] placeholders where values are missing, never fabricated → flagged regulatory-compliance points — all first drafts for qualified scientific or medical review.

// 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.