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 WritingMaster the art of transforming complex clinical trial data into clear, compliant, and patient-friendly lay...
₹90,000
Foundations of Regulatory Medical WritingBuild a strong foundation in regulatory medical writing by mastering the structure, purpose, and compliance...
₹75,000
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