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.
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Clinical & Medical Summary Writing
Master the art of transforming complex clinical trial data into clear, compliant, and patient-friendly lay summaries.
₹90,000 -
Foundations of Regulatory Medical Writing
Build a strong foundation in regulatory medical writing by mastering the structure, purpose, and compliance requirements of core clinical trial documents.
₹75,000 -
Lab to Label – Translating Science into Approved Therapies
Understand the end-to-end journey of a drug from discovery to market label, and the writer’s critical role in shaping regulatory and scientific documents at every stage.
₹110,000 -
Strategic Review in Medical & Regulatory Writing
Go beyond grammar checks and master the art of strategic review to strengthen scientific clarity, regulatory acceptability, and submission quality.
₹80,000 -
CSR Writing Masterclass – From Protocol to Submission
Gain proficiency in authoring ICH E3-compliant Clinical Study Reports (CSRs) that are clear, accurate, and submission-ready.
₹50,000 -
AI for Medical & Regulatory Writers
Harness the power of AI to elevate your medical writing, compliance, and quality assurance skills for the future of pharma documentation.
₹60,000