If you are interested in becoming a regulatory affairs professional but have no experience, or if you are working as a regulatory affairs professional but would like to have a strong foundation on the basics of regulatory affairs, then this course is suitable for you. This is the most comprehensive regulatory affairs course available, providing you with a strong foundation in regulatory affairs by increasing your baseline knowledge through the comprehensive lecture series, as well as offering case studies. The comprehensive lecture series covers EU, US and UK regulations across the whole product lifecycle, from clinical trials through to marketing authorisation applications and variations. Moreover medical device regulations and clinical/medical regulatory affairs are also covered. Additionally, you will join the exclusive professional community and receive job search support. This course will provide you with the fundamentals of regulatory affairs in the EU, US and UK. It is run by our experts who have considerable experience in pharmaceutical companies and regulatory health authorities. To access the full lecture series, CV review, interview preparation, work experience assignments and access to an exclusive professional community, see the full introductory course. Invest in your self and start your professional journey today.
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