Medical Device Hardware Manual Writing
Budget: ₹750 – ₹1,250 INR
I have a new medical-grade piece of hardware coming to market and I need a clear, compliant English user manual that guides clinicians and biomedical engineers through installation, operation, maintenance, and basic troubleshooting. This is strictly technical documentation, not marketing copy or a blog, so every paragraph must be precise, unambiguous, and aligned with current medical-device standards (ISO 13485 terminology, IEC 60601 references, etc. where relevant).
You will work from engineering drawings, exploded views, and draft procedures that I will supply in PDF and STEP formats. The final deliverable should be a fully formatted Word document (and PDF) with:
• Sectioned layout: safety information, technical specifications, step-by-step procedures, warnings/cautions, cleaning/sterilisation, and service guidelines
• Consistent numbered headings, figure captions and cross-references
• Tables and bullet lists redrawn for clarity
• American or British English—let me know your preference before we begin
Acceptance criteria
1. All procedures reproduce exactly the intent of the source material with zero ambiguity.
2. Terminology matches the device labelling and GUI.
3. Document passes Grammarly Premium with under 2 % passive voice and no critical errors.
4. Ready-to-print PDF plus an unlocked Word file delivered.
If you have previous experience writing for medical devices, especially for regulatory submissions, that will be a strong plus. I’m ready to start as soon as I review a short sample of your past technical manuals or a 200-word extract rewritten from my draft.
You will work from engineering drawings, exploded views, and draft procedures that I will supply in PDF and STEP formats. The final deliverable should be a fully formatted Word document (and PDF) with:
• Sectioned layout: safety information, technical specifications, step-by-step procedures, warnings/cautions, cleaning/sterilisation, and service guidelines
• Consistent numbered headings, figure captions and cross-references
• Tables and bullet lists redrawn for clarity
• American or British English—let me know your preference before we begin
Acceptance criteria
1. All procedures reproduce exactly the intent of the source material with zero ambiguity.
2. Terminology matches the device labelling and GUI.
3. Document passes Grammarly Premium with under 2 % passive voice and no critical errors.
4. Ready-to-print PDF plus an unlocked Word file delivered.
If you have previous experience writing for medical devices, especially for regulatory submissions, that will be a strong plus. I’m ready to start as soon as I review a short sample of your past technical manuals or a 200-word extract rewritten from my draft.