AI for Medical & Regulatory Writers

Harness the power of AI to elevate your medical writing, compliance, and quality assurance skills for the future of pharma documentation.

Functions

Legal/ RegulatoryQualityR&D
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2 day

Program Overview

This course empowers medical and regulatory writers to responsibly integrate AI tools into their everyday workflows, covering prompt engineering, ethical and regulatory compliance, and quality control in AI-assisted writing. Through practical demos, real-world exercises, and future-focused insights, participants will learn to confidently blend human expertise with machine intelligence, ensuring accuracy, compliance, and relevance as the medical writing profession evolves in the era of generative AI.

Features

  • Understand and apply leading AI tools in regulatory and scientific writing.
  • Design effective prompts and workflows for content creation and quality control.
  • Navigate compliance standards for AI-assisted documentation.
  • Develop strategies for ethical, human-in-the-loop, and futureproof adoption of AI in pharma writing.

Target audiences

  • Regulatory, scientific, and medical writers
  • QC Professionals
  • Pharma L&D professionals

Curriculum

  • 7 Sections
  • 21 Lessons
  • 2 Days
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Instructor

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Nomita Saxena

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An experienced regulatory writing consultant, she brings 20+ years in medicine and pharma R&D, with leadership roles at AstraZeneca, Novo Nordisk, and Accenture. She specializes in clinical and regulatory documentation and now partners with global clients to deliver high-impact content and capability-building programs.

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