Scientific and Medical Writing Essentials for Pharmaceuticals

Master the essential scientific writing skills required to produce impactful, compliant, and publication-ready documents in the pharma and healthcare industry.

Functions

Legal/ RegulatoryOperationsR&D
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1 day

Program Overview

In today’s rapidly evolving healthcare landscape, medical and scientific writing plays a pivotal role in bridging the gap between scientific innovation and clinical application. Whether it’s regulatory documentation, clinical study reports, or scientific publications, the need for clear, accurate, and compliant communication has never been greater. This program is tailored for mid and junior-level pharmaceutical professionals aiming master the core scientific writing skills and industry knowledge required to craft high-quality, impactful content that supports drug development, regulatory approval, and scientific engagement across global Pharma, Biotech, and MedTech sectors. Led by an industry expert with over 20 years of experience, the course emphasizes practical learning through real-life examples, case studies, and hands-on activities. Participants will gain proficiency in crafting various publication documents, including original articles, review articles, clinical study reports (CSRs), abstracts, plain language summaries (PLS), and scientific congress materials. The program also offers live demonstrations on literature search techniques and introduces the latest tools to streamline the writing process. 

Features

  • Master Best Practices in Scientific Documentation: Learn to write clear, concise, and compliant technical documents tailored for diverse stakeholders.
  • Enhance Operational Efficiency: Acquire practical techniques to ensure accuracy, traceability, and consistency in documentation.
  • Ensure Adherence to Industry Standards: Develop skills to review and edit documents aligning with regulatory and operational guidelines.
  • Apply Knowledge Practically: Engage with real-world examples and case studies to reinforce learning.

Target audiences

  • Medical and Regulatory Affairs Associates
  • Clinical Research Professionals
  • Healthcare Communication Specialists

Instructor

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Shelly Arora

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An Independent Trainer and Medical Communications Consultant with 20+ years of experience in pharma and healthcare, specialized in scientific writing, regulatory documentation, and advisory board communications. Has held senior leadership roles at Indegene, WNS, Knowledge Isotopes, and Turacoz Healthcare Solutions, led high-performing teams and contributed to business development and strategic communication initiatives. Today, I consult with pharma professionals and organizations, offering expert insights and creating impactful, customized content to elevate scientific engagement and communication.

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