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.
Lab to Label – Translating Science into Approved TherapiesUnderstand the end-to-end journey of a drug from discovery to market label, and the writer’s…
₹110,000
Strategic Review in Medical & Regulatory WritingGo beyond grammar checks and master the art of strategic review to strengthen scientific clarity,…
₹80,000
CSR Writing Masterclass – From Protocol to SubmissionGain proficiency in authoring ICH E3-compliant Clinical Study Reports (CSRs) that are clear, accurate, and…
₹50,000
AI for Medical & Regulatory WritersHarness the power of AI to elevate your medical writing, compliance, and quality assurance skills…
₹60,000