{"product_id":"nora-medical-writer-ai-skill","title":"Nora — Medical Writer AI Skill","description":"\u003cdiv style=\"font-family: 'DM Sans', sans-serif; color: #1A1A18; max-width: 680px;\"\u003e\n\n  \u003cp style=\"font-size: 16px; font-weight: 600; color: #1A1A18; line-height: 1.5; margin: 0 0 8px 0;\"\u003e\n    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.\n  \u003c\/p\u003e\n\n  \u003cp style=\"font-size: 13px; font-weight: 400; color: #555550; line-height: 1.7; margin: 0 0 28px 0;\"\u003e\n    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.\n  \u003c\/p\u003e\n\n  \u003cdiv style=\"background: #F0EAFE; border-radius: 12px; padding: 24px 28px; margin-bottom: 24px;\"\u003e\n    \u003cp style=\"font-size: 10px; font-weight: 600; color: #6B3FE0; letter-spacing: 0.08em; text-transform: uppercase; margin: 0 0 16px 0;\"\u003eWhat you get\u003c\/p\u003e\n    \u003cul style=\"margin: 0; padding: 0; list-style: none;\"\u003e\n      \u003cli style=\"font-size: 13px; color: #1A1A18; padding: 7px 0; border-bottom: 1px solid rgba(107,63,224,0.12); display: flex; align-items: flex-start; gap: 10px;\"\u003e\n        \u003cspan style=\"color: #6B3FE0; font-weight: 600; flex-shrink: 0;\"\u003e→\u003c\/span\u003e\n        \u003cspan\u003eRegulatory 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\u003c\/span\u003e\n      \u003c\/li\u003e\n      \u003cli style=\"font-size: 13px; color: #1A1A18; padding: 7px 0; border-bottom: 1px solid rgba(107,63,224,0.12); display: flex; align-items: flex-start; gap: 10px;\"\u003e\n        \u003cspan style=\"color: #6B3FE0; font-weight: 600; flex-shrink: 0;\"\u003e→\u003c\/span\u003e\n        \u003cspan\u003eClinical 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\u003c\/span\u003e\n      \u003c\/li\u003e\n      \u003cli style=\"font-size: 13px; color: #1A1A18; padding: 7px 0; border-bottom: 1px solid rgba(107,63,224,0.12); display: flex; align-items: flex-start; gap: 10px;\"\u003e\n        \u003cspan style=\"color: #6B3FE0; font-weight: 600; flex-shrink: 0;\"\u003e→\u003c\/span\u003e\n        \u003cspan\u003ePublications 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\u003c\/span\u003e\n      \u003c\/li\u003e\n      \u003cli style=\"font-size: 13px; color: #1A1A18; padding: 7px 0; border-bottom: 1px solid rgba(107,63,224,0.12); display: flex; align-items: flex-start; gap: 10px;\"\u003e\n        \u003cspan style=\"color: #6B3FE0; font-weight: 600; flex-shrink: 0;\"\u003e→\u003c\/span\u003e\n        \u003cspan\u003ePatient-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\u003c\/span\u003e\n      \u003c\/li\u003e\n      \u003cli style=\"font-size: 13px; color: #1A1A18; padding: 7px 0; border-bottom: 1px solid rgba(107,63,224,0.12); display: flex; align-items: flex-start; gap: 10px;\"\u003e\n        \u003cspan style=\"color: #6B3FE0; font-weight: 600; flex-shrink: 0;\"\u003e→\u003c\/span\u003e\n        \u003cspan\u003eMedical 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\u003c\/span\u003e\n      \u003c\/li\u003e\n      \u003cli style=\"font-size: 13px; color: #1A1A18; padding: 7px 0; display: flex; align-items: flex-start; gap: 10px;\"\u003e\n        \u003cspan style=\"color: #6B3FE0; font-weight: 600; flex-shrink: 0;\"\u003e→\u003c\/span\u003e\n        \u003cspan\u003eHealth 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\u003c\/span\u003e\n      \u003c\/li\u003e\n    \u003c\/ul\u003e\n  \u003c\/div\u003e\n\n  \u003cdiv style=\"display: flex; align-items: center; gap: 20px; background: #FFFFFF; border: 1px solid #E8E6E0; border-radius: 8px; padding: 14px 20px; margin-bottom: 24px;\"\u003e\n    \u003cspan style=\"font-size: 11px; color: #888780; font-family: monospace;\"\u003e📄 nora-medical-writer.md\u003c\/span\u003e\n    \u003cdiv style=\"width: 1px; height: 16px; background: #E8E6E0;\"\u003e\u003c\/div\u003e\n    \u003cspan style=\"font-size: 11px; color: #888780;\"\u003eUnder 2 min install\u003c\/span\u003e\n    \u003cdiv style=\"width: 1px; height: 16px; background: #E8E6E0;\"\u003e\u003c\/div\u003e\n    \u003cspan style=\"font-size: 11px; color: #888780;\"\u003eWorks with Claude Sonnet 4 \u0026amp; Claude Cowork\u003c\/span\u003e\n  \u003c\/div\u003e\n\n  \u003cdiv style=\"border-left: 3px solid #6B3FE0; padding-left: 16px;\"\u003e\n    \u003cp style=\"font-size: 10px; font-weight: 600; color: #6B3FE0; letter-spacing: 0.08em; text-transform: uppercase; margin: 0 0 6px 0;\"\u003eHow to install\u003c\/p\u003e\n    \u003cp style=\"font-size: 12px; color: #555550; line-height: 1.7; margin: 0;\"\u003e\n      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.\n    \u003c\/p\u003e\n  \u003c\/div\u003e\n\n\u003c\/div\u003e","brand":"Kissmyskills","offers":[{"title":"Default Title","offer_id":57638819758344,"sku":null,"price":29.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1036\/1444\/7880\/files\/08_nora-medical-writer.png?v=1776861282","url":"https:\/\/kissmyskills.com\/products\/nora-medical-writer-ai-skill","provider":"KissMySkills","version":"1.0","type":"link"}