Overview
Course Description:
Our Regulatory Affairs Course teaches you how to navigate drug approval processes, regulatory submissions, and compliance requirements across major markets like the US FDA, EMA, and CDSCO. Learn to prepare dossiers, CTD/eCTD submissions, and manage product life-cycle compliance. Ideal for professionals aiming to work in pharmaceutical companies, medical device firms, and regulatory consultancies.
Keywords: regulatory affairs course in India, US FDA training, drug approval process training, CTD eCTD course, regulatory compliance jobs, regulatory affairs certification.
Course Features
- Lecture 0
- Quiz 0
- Duration 10 weeks
- Skill level All levels
- Language English
- Students 0
- Assessments Yes
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