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Nomita Saxena
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.
- Clinical & Medical Summary Writing1 DayJunior Professionals18 Lessons0 Quizzes0 Students
Master the art of transforming complex clinical trial data into clear, compliant, and patient-friendly lay…
₹90,000 - Foundations of Regulatory Medical Writing1 DayJunior Professionals29 Lessons0 Quizzes0 Students
Build a strong foundation in regulatory medical writing by mastering the structure, purpose, and compliance…
₹75,000 - Lab to Label – Translating Science into Approved Therapies3 DaysJunior Professionals28 Lessons0 Quizzes0 Students
Understand the end-to-end journey of a drug from discovery to market label, and the writer’s…
₹110,000 - Strategic Review in Medical & Regulatory Writing1 DayMid-Senior Professionals31 Lessons0 Quizzes0 Students
Go beyond grammar checks and master the art of strategic review to strengthen scientific clarity,…
₹80,000 - CSR Writing Masterclass – From Protocol to Submission1 DayMid-Senior Professionals19 Lessons0 Quizzes0 Students
Gain proficiency in authoring ICH E3-compliant Clinical Study Reports (CSRs) that are clear, accurate, and…
₹50,000 - AI for Medical & Regulatory Writers2 DaysJunior Professionals21 Lessons0 Quizzes0 Students
Harness the power of AI to elevate your medical writing, compliance, and quality assurance skills…
₹60,000