Description

A professionally structured Medical Writing Plan Template tailored for clinical research teams, CROs, and freelance medical writers. This editable document complies with ICH E3, ICH GCP, and industry-standard SOPs.

Perfect for Phase I–III clinical trials, this partially customized template provides the structure, regulatory references, and example content needed to save hours of formatting and regulatory guesswork.

📦 What’s Included:

• 🗂️ Editable Word (.docx) template

• 📑 Fully structured Table of Contents

• 📋 Pre-filled example content in each section

• 🔒 ICH E3 and GCP compliance references

🎯 Who It’s For:

• Clinical research professionals

• Medical writing consultants & freelancers

• CROs & biotech project teams

• Regulatory affairs & quality teams

• ✅ Compatible with TMF and eCTD submissions

💡 Key Benefits:

• ✅ Saves 5–10 hours of formatting time

• ✅ Easy to customize for each protocol

• ✅ Ensures audit-ready document trail

• ✅ Helps align with SOPs and regulatory requirements

📥 Download Format:

• Microsoft Word (.docx)

• Instant digital download after purchase

🔄 License:

• Personal & professional use

• Unlimited projects

• Not for resale or distribution

🔐 Refund Policy:

Due to the digital nature of this product, all sales are final.