MasterMedicalWriting
120-hour hands-on program — from preclinical documents to regulatory submissions. Job-ready from day one.
Our Mission
We empower life-science graduates to develop the confidence, the mindset, and the hands-on writing skills required to succeed in the global medical writing and clinical research job market.
02 / Writing Domains
End-to-end writing across
the product lifecycle.
Every document type you will encounter in a medical writing career — written, reviewed, and mastered during training.
Preclinical Writing
Study reports, pharmacology summaries, toxicology write-ups — the foundation of the drug development dossier.
Clinical Trial Writing
Protocols, Clinical Study Reports (CSR), Informed Consent Forms (ICF), Investigator Brochures (IB).
Regulatory Submissions
CTD/eCTD modules, NDA/BLA/MAA documents, Module 2 summaries.
Safety & Pharmacovigilance
ICSRs, PSURs, Risk Management Plans, signal detection narratives.
Scientific Publications
Journal manuscripts, poster abstracts, conference presentations following ICMJE guidelines.
Style Guides & Lay Summaries
AMA/APA referencing, writing style guides, lay summaries for patients.
03 / Faculty
Trained by practising
industry experts.
Dr. Selvastine Selvaraj
DVM MVSc
A practising veterinary professional and medical writing specialist with deep expertise in preclinical and clinical documentation. Dr. Selvastine founded Elwords to bridge the gap between academic life sciences education and the demanding standards of the global medical writing industry. His training is built on real documents, real guidelines, and real industry expectations.
Dr. Adesh Saxena
PhD
A seasoned researcher and industry expert based in the USA with extensive experience in global clinical research and regulatory affairs. Dr. Adesh brings an international perspective to the program, ensuring learners are prepared for opportunities across US, EU, and global markets.
04 / Programs
One foundation.
Three advanced paths.
Start with our 2-day foundation course or dive deep with a 15-day advanced program tailored to your specialisation.
Foundation in Medical Writing
An intensive 2-day course covering the fundamentals of medical writing for life-science graduates and professionals.
Documents You Will Write
Introduction to Medical Writing
Overview of the medical writing profession and career pathways
Regulatory Framework Basics
ICH guidelines, FDA, EMA — understanding the regulatory landscape
Document Types Overview
Key document categories across the product lifecycle
Writing Style & Language
Scientific writing principles, clarity, precision, and conciseness
Referencing & Style Guides
AMA/APA referencing, in-text citations, and bibliography
Hands-on Writing Exercise
Practical writing session with real-world document templates
05 / Career Outcomes
Companies that hire
medical writers.
A trained medical writer is sought across pharma, devices, CROs, and healthcare IT — globally.
60%
of medical writers work in pharma
Pharmaceutical Companies
Regulatory affairs, clinical operations, and medical writing teams at pharma companies ranging from generics to innovators.
#1
employer category globally
Contract Research Organisations
CROs are the largest employers of medical writers globally, offering exposure to diverse therapeutic areas and clients.
35%
faster growing than pharma writing
Medical Device Companies
Module 2 training prepares you specifically for regulatory writing roles at Class II and Class III device companies.
2x
salary premium for trained writers
ITES-Healthcare & Publishing
Medical communications agencies, scientific publishing firms, and healthcare IT companies all hire trained medical writers.
06 / Register
Start your medical
writing career today.
Direct Contact
Dr. Selvastine Selvaraj
DVM MVSc
Founder, Trainer & Consultant
Program Highlights
- 120 hours of structured training
- Hands-on writing — real documents
- End-to-end product lifecycle coverage
- Medicine, Biologics & Device writing
- Style guides, referencing, lay summaries
- Job-oriented curriculum design