Medical Writing Course in Kentucky

Medical Writing Course in Kentucky

  • ★ ★ ★ ★ ★ 4.8/5 Ratings
  • 1.1 Million Learners
  • 1649 Learner’s Rating
  • 81% Report Career Benefits

Learn Scientific Writing a foundational course at your own pace | Learn to write documents such as medical case reports, scientific news, journals, etc | Organize and present scientific information for different audiences

Starts In 2 day

18 May 2024

Learning Period

24 Hours

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There's a reason that 95% of our alumni undertake 3+ courses as a minimum with Henry Harvin®

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Know the complete offerings of our Medical Writing Course in Kentucky

Key Highlights

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Facility to undergo various projects along with the course.

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Free access to the E-learning Portal and future updates. Get access to PPTs, Projects, Quizzes, self-paced Video-based learning, a question bank, a library, practice tests, final assessment, a forum, and doubt sessions.

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Mentorship from Young Successful Entrepreneurs to set up a sustainable & scalable Business from scratch at both Freelance and entrepreneur levels

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Medical Writing Course Curriculum

  • Module 1: Introduction to Medical Writing

    This module will equip the candidate with the basics of Medical Writing. Gain skillsets and motivation required for medical writing. Know about the scope & Necessities of medical writing. Learn about the categories of Medical Writing and Core Areas in Medical Writing: Consumer Insights & Requirements
    • Understanding the term ‘Medical Writing’
    • Skillsets & Motivation required for Medical Writing
    • Scope & Necessities of Medical Writing
    • Valuable Salient Features
    • Planning & Layout for Medical Writing
    • Categories of Medical Writing
    • Core Areas in Medical Writing: Consumer Insights & Requirements
    • Quiz Module 1
  • Module 2: Scientific Writing

    This module will help the candidate with the knowledge of Scientific Writing. Gain understanding about the Scientific news and reviews. Know extensively about the Scientific Research paper for journals
    • Scientific News
    • Scientific Reviews
    • Scientific Research Paper for Journals
    • Case Reports
    • Quiz Module 2
  • Module 3: Drug Development Process-An Overview

    This module will help the candidate with the knowledge of drug development process. Learn about the Pr-Clinical Development and Clinical Research. Gain understanding about the Clinical study designs and Post-marketing surveillance
    • Pre-clinical Development
    • Clinical Development / Research
    • Clinical Study Designs
    • Post-Marketing Surveillance
    • Quiz Module 3
  • Module 4: Pre-clinical/ Non-Clinical Writing

    This module will guide you through the knowledge of Pre-Clinical or Non-clinical writing, Know the differences between clinical and non-clinical writing. Learn about the International Conference on Harmonisation (ICH) Guidelines. Gain understanding about the good laboratory practices, Non-clinical summaries, non-clinical study reports, and more
    • Differences between Clinical and Non-Clinical Writing
    • About The International Conference on Harmonisation (ICH) Guidelines
    • Good Laboratory Practices
    • Non-clinical Summaries
    • Non-clinical Study Reports
    • Quiz Module 4
  • Module 5: Medical Writing for Clinical Trial

    This module will guide the candidate with Medical Writing for Clinical Trial. Know about the Investigational Medical Product dossiers, investigator's brochure, and more. Learn about protocol writing and informed consent. Gain knowledge about the Development Safety Update Report, Report amendments, and updates
    • Investigational Medicinal product dossiers
    • The Investigators Brochure
    • Protocol writing
    • Informed Consent
    • DSUR (Development Safety Update Report)
    • Report amendments and updates
    • Data Analytics
    • Quiz Module 5
  • Module 6: Medical Writing in post-marketing phase

    This module will guide the candidate with comprehensive knowledge of medical writing in the post-marketing phase. Learn about creating Risk management plans and Aggregate reports. Know about the CSR, CER, PSUR, and PER
    • Aggregate Reports
    • Risk Management Plans (RMPs)
    • CSR (Clinical Study Report)
    • CER (Clinical Evaluation Report)
    • PSUR (Periodic Safety Update Report)
    • PER (Performance Evaluation Report)
    • Quiz Module 6
  • Module 7: Guidelines to Publish Clinical Data

    This module will guide the candidate with the knowledge of Guidelines to publish Clinical Data. Know all the guidelines such as CONSORT, TREND, STROBE, CARE, COREQ, PRISMA, MOOSE, STARD, TRIPOD, and more
    • CONSORT (Consolidated Standard of Reporting Trials)
    • TREND (Technology Recreation Education Nature and Discovery)
    • STROBE (STrengthening the Reporting of OBservational studies in Epidemiology)
    • CARE (Compassion, Advocacy, Restoration, and Educational)
    • COREQ (COnsolidated criteria for REporting Qualitative research)
    • PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses)
    • MOOSE (Meta-analysis of Observational Studies In Epidemiology)
    • STARD (Standards for Reporting of Diagnostic accuracy studies)
    • TRIPOD (Transparent Reporting of a multivariable prediction model for Individual Prognosis or Diagnosis)
    • Quiz Module 7
  • Module 8: Pharmacovigilance

    In this module the candidate will learn about methodologies in Pharmacovigilance. Gain extensive knowledge about the Drug Dictionary and PVPI. Know the Pharmcovigilance Compliance & Inspections
    • Methodologies in Pharmacovigilance
    • How to Create Template Paragraph Styles?
    • Pharmacovigilance Programme in India (PVPI)
    • Pharmacovigilance of Herbal Drugs & Medical Devices
    • Pharmacovigilance compliance & Inspections
    • Quiz Module 8
  • Module 9: Regulatory Strategies

    In this module, the candidate will know about the Regulatory Strategies in different phases of a Clinical Trial. Know the Fundamnetals of Patent and writing of regulatory submissions and drug protection activities
    • Regulatory Strategies in different phases of a Clinical Trial
    • Writing for Regulatory submissions and Drug Protection Activities (IND, NDA, BLA, SNDA, ANDA)
    • Patent- Fundamental Concept
    • Quiz Module 9
  • Module 10: Techniques And Models For Medical Writing

    • Six Scientific Techniques for Medical Writing
    • Readers Checklist: Editing & Reviewing
    • Cooperative Principles and their Requirements
    • Models for Medical Writing: Telescope and Exposition
    • Instruction for Medical / Clinical / Regulatory Writing
    • Mosaic Structure & Layout
    • Clinical Evaluation Report (CER)
    • Periodic Safety Update Report (PSUR)
    • Performance Evaluation Report (PER)
    • Quiz Module 10
  • Module 11: Complimentary Module 1: Soft Skills Development

    • Business Communication
    • Preparation for the Interview
    • Presentation Skills
  • Module 12: Complimentary Module 2: Resume Writing

    • Resume Writing

Know the complete offerings of our in Medical Writing Course

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