Healthcare & Medical

Professional Medical Writing Certification Program

Enhance your career in healthcare by mastering the art of medical writing.

Clinical and regulatory document preparation — learn to draft protocols, informed consent forms, clinical study reports, and submission-ready regulatory documents. Scientific communication and publication skills — master writing manuscripts, abstracts, posters, and clear evidence-based summaries for diverse audiences. Practical, hands-on learning — real-world examples, templates, structured assignments, and feedback to build portfolio-ready deliverables.
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Signature Learning Experience
Professional Medical Writing Certification Program
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Earn an industry-recognized credential and get access to mentor-led guidance throughout your learning journey.

4.9/5 Program Rating
1,765 Learners Enrolled
All level Level
32 hrs Total Duration
English,Hindi Language
Program Overview

Experience a modern, outcome-driven curriculum

Built with industry mentors, this program blends immersive live sessions, simulation projects, and on-demand resources so you can master Mandarin Chinese with confidence.

This comprehensive course on medical writing covers everything from clinical trial protocols to regulatory document preparation. Explore best practices and real-world applications in a structured format.

Why learners love this program

Each element is crafted to accelerate fluency, cultural context, and career readiness.

  • Clinical and regulatory document preparation — learn to draft protocols, informed consent forms, clinical study reports, and submission-ready regulatory documents.
  • Scientific communication and publication skills — master writing manuscripts, abstracts, posters, and clear evidence-based summaries for diverse audiences.
  • Practical, hands-on learning — real-world examples, templates, structured assignments, and feedback to build portfolio-ready deliverables.
Lectures
16
Guided Hours
32 hrs.
Program Investment
₹12,500
Learning Outcomes

Unlock the capabilities that matter in real-world communication

Every module stacks practical language skills with cultural fluency, so you can speak confidently in professional, academic, and social settings.

Understand the role and scope of medical writing across clinical, regulatory, and promotional contexts
Differentiate types of medical documents (protocols, clinical study reports, informed consent forms, regulatory submissions, manuscripts, abstracts, posters, and patient materials)
Apply principles of clear, accurate, and audience-appropriate scientific writing
Design and write clinical trial protocols and clinical study reports in line with ICH-GCP, CONSORT, and applicable guidelines
Prepare regulatory submission documents (e.g., CTD modules) and understand regulatory expectations and timelines
Conduct literature searches, perform critical appraisal, and manage references and citations correctly
Create and format tables, figures, and statistical displays to communicate data effectively
Draft manuscripts and abstracts for peer-reviewed journals and manage the journal submission and peer-review process
Implement ethical standards including authorship criteria, conflict of interest disclosure, and plagiarism avoidance
Edit and peer-review documents for clarity, consistency, and compliance using version control and quality-check workflows
Collaborate effectively with multidisciplinary teams (clinicians, statisticians, regulatory affairs, CROs) and manage project timelines
Use authoring and reference-management tools (e.g., EndNote, Mendeley, track changes) and apply AI-assisted writing tools responsibly
Certificate

Certificate You'll Receive

Earn an industry-recognized certificate upon successful completion of this course.

Professional Medical Writing Certification Program — Course Certificate
Personalised guidance

Book a discovery call with our program specialists

Get tailored advice on learning paths, certification journeys, and industry opportunities before you enroll.

In a focused 20-minute consultation we map your current proficiency, clarify where you want to get to, and suggest the quickest route to fluency with milestones we can help you hit.

  • Understand the skill gaps holding you back and the modules that can close them in the next cohort.
  • Get a personalised cohort recommendation based on availability, trainer profile, and your weekly bandwidth.
  • Discover global project work and certification add-ons that enhance Mandarin credentials on your CV.

Reserve your slot

Share your details and we will connect within 24 hours to set up a personalised walkthrough.

Curriculum Architecture

Structured modules that build fluency session after session

Explore the complete roadmap—from foundational vocabulary to advanced professional expressions—crafted with practical immersion in mind.

Role and Scope of Medical Writing
Explain the role and scope of medical writing within healthcare, research, and industry settings. Identify key stakeholders and common document types.
1.50 hrs
Career Paths and Professional Skills
Describe common career paths, required competencies, and professional development opportunities in medical writing. Outline essential skills such as scientific literacy, editing, and project management.
1.50 hrs

Regulatory, Scientific, and Marketing Writing
Differentiate the goals, audiences, and constraints of regulatory, scientific, and marketing medical writing. Provide examples of typical documents in each category.
1.50 hrs
Audience and Purpose
Assess how audience and purpose influence tone, structure, and content of medical documents. Apply audience analysis to tailor messaging appropriately.
1.50 hrs
Document Types Overview
Survey common document types across settings, including protocols, manuscripts, patient materials, and regulatory submissions. Match document types to typical workflows and timelines.
1.50 hrs

Protocol Structure and Essential Elements
Identify and describe the standard sections and required elements of a clinical trial protocol. Explain the rationale for each section and how they interrelate.
1.50 hrs
Study Design and Safety Considerations
Explain key design elements such as objectives, endpoints, randomization, and blinding. Discuss safety monitoring, adverse event reporting, and risk mitigation language.
1.50 hrs

Principles of Ethical Consent Writing
Summarize ethical and regulatory principles underpinning informed consent documents. Ensure consent language supports participant autonomy and comprehension.
1.50 hrs
Clear Language and Layout Strategies
Apply plain language techniques and document design to improve participant understanding. Create consent templates that balance completeness with readability.
1.50 hrs

IND and BLA Requirements
Outline the content and structure expectations for Investigational New Drug (IND) and Biologics License Application (BLA) submissions. Identify key regulatory guidelines and common pitfalls.
1.50 hrs
Compilation and Formatting for Submissions
Describe best practices for compiling modules, templates, and submission-ready documents. Apply consistent formatting and indexing to meet regulatory requirements.
1.50 hrs
Responding to Regulatory Queries
Develop strategies for drafting clear, evidence-based responses to regulatory questions and requests for information. Coordinate document versions and audit trails during exchanges.
1.50 hrs

Manuscript Structure and Authorship
Explain the structure of a scientific manuscript and criteria for authorship and contributorship. Draft clear objectives, methods, results, and discussion sections.
1.50 hrs
Peer Review and Submission Process
Navigate the peer review and journal submission process, including cover letters and revision responses. Implement strategies to handle reviewer feedback constructively.
1.50 hrs

Plain Language Techniques
Use plain language principles to translate technical content into accessible patient-facing text. Test readability and comprehension for diverse patient populations.
1.50 hrs
Designing Patient-Facing Materials
Combine text, visuals, and layout to create effective educational and consent materials for patients. Ensure cultural sensitivity and health literacy considerations are integrated.
1.50 hrs

Plagiarism, Authorship, and Disclosure
Recognize ethical issues such as plagiarism, ghostwriting, and authorship disputes. Apply disclosure and attribution best practices to maintain integrity.
1.50 hrs
Ethical Case Studies and Decision-Making
Analyze real-world ethical scenarios to practice decision-making and conflict resolution. Implement policies that promote transparency and accountability.
1.50 hrs

Citation Styles and Reference Management
Compare common citation styles (e.g., AMA, Vancouver) and select appropriate formats for different documents. Use reference management tools to organize and format citations.
1.00 hrs
Avoiding Common Referencing Errors
Identify and correct typical referencing mistakes, including incorrect citations and missing references. Ensure accuracy and traceability of sources in manuscripts and regulatory documents.
1.50 hrs

Project Planning and Drafting
Develop a project plan that integrates course concepts into a complete medical writing piece and produce an initial draft. Define scope, audience, and timeline for the final submission.
1.00 hrs
Revision, Presentation, and Peer Feedback
Refine the draft through structured revision and incorporate peer and instructor feedback. Present the final document and reflect on lessons learned and areas for improvement.
1.50 hrs
Upcoming Batches

Pick a schedule that fits your routine

We run multiple live cohorts so you can line up a batch with your goals, weekly bandwidth, and preferred mode of learning.

Weekend Batch Filling fast

Starts 27 Sep 2025

  • 08:00 AM - 10:00 AM
  • Morning Batch
  • SS cadence
  • 16 live sessions
Weekend Batch

Starts 27 Sep 2025

  • 08:00 PM - 10:00 PM
  • Evening Batch
  • SS cadence
  • 16 live sessions
Weekday Batch

Starts 29 Sep 2025

  • 08:00 AM - 10:00 AM
  • Morning Batch
  • MWF cadence
  • 16 live sessions
Weekday Batch

Starts 29 Sep 2025

  • 08:00 PM - 10:00 PM
  • Evening Batch
  • MWF cadence
  • 16 live sessions
Weekend Batch

Starts 04 Oct 2025

  • 08:00 AM - 10:00 AM
  • Morning Batch
  • SS cadence
  • 16 live sessions
Weekend Batch

Starts 04 Oct 2025

  • 08:00 PM - 10:00 PM
  • Evening Batch
  • SS cadence
  • 16 live sessions
Learner Voices

Stories from professionals who accelerated with SkillsBiz

Hear how learners leveraged mentor feedback, immersive projects, and certification support to reach their Mandarin goals.

D
Divya Tiwari
The sessions were detailed and easy to follow. The trainer gave examples from real clinical studies, which helped me understand how theory is applied in practice. This approach made the entire learning process both interesting and useful.
N
Navneet Kaur
The training gave me practical exposure to medical writing. Working on research summaries and clinical documents gave me real confidence. I can now draft and review documents with much more accuracy and professionalism.
S
Shweta Raghavan
The Medical Writing program was well-structured and comprehensive. The trainer focused on documentation standards, editing, and formatting, which are crucial for this field. With consistent practice, I now feel confident to start my career in medical writing.
V
Vivek Raina
The course gave me a strong foundation in research-based writing. The trainer explained even the most technical concepts with patience, making it easy for beginners like me to understand. I gained both confidence and clarity, which I was lacking before.
I
Imtiaz Khan
The program was very practical and focused on real industry needs. I especially liked how regulatory writing and literature review were taught with examples. The research summary exercises made me confident that I can handle professional assignments in medical writing.
R
Rajeev Menon
Joining the Medical Writing course was the right choice. The trainer explained scientific documentation, clinical reports, and research writing in a very clear manner. The gradual approach helped me build confidence, and I now feel ready to apply these skills professionally.
Frequently Asked Questions

Your questions, answered in one place

Everything you need to know before you commit—from certification timelines to support during the program.

The course lasts for 32 hours.
The course costs 12500.
This course is designed for individuals at an intermediate level.
The course is delivered in English.
Yes, a certificate of completion will be awarded after successfully finishing the course.
Some prior knowledge in healthcare or life sciences is recommended.
Yes, you will have continued access to course materials after completion.
This course is geared towards intermediate learners, so prior experience in medical writing is beneficial.
The curriculum includes lectures on various aspects of medical writing, practical exercises, and a final project.
The course will be taught by experienced professionals in the medical writing field.

Global recognitions that power your profile

We are trusted by leading accreditation bodies, ensuring your certificate is respected by employers worldwide.

Nasscom Certification ISO Certification MSME Certification ISO 9001 Certification Startup India Certification EU Certification MCA Certification Future Skills Certification
Awards & Recognitions

Celebrated for excellence in outcome-driven education

Our pedagogy, learner outcomes, and mentor network have been acknowledged by industry councils and global education forums.

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