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Regulatory Affairs for Support Staff Training Course
You basket is empty. The Regulatory Affairs Training Course for Support Staff. The Regulatory Affairs for Support Staff training course will cover the following: European law – directives, regulations and guidelines. Where can I find information about regulatory requirements? The Drug Development Process. Clinical Trials in Europe In Europe, you can seek scientific advice. The types and categories of marketing authorization applications.
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This two-day training course is designed for support staff who are interested in learning about pharmaceutical regulatory affairs.
The course is highly recommended for anyone who wants to know more about the regulations they are involved in.
24-25 September 2024From PS1099.
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The role of a pharmaceutical regulatory affairs professional is challenging. It involves involvement in drug development, marketing authorization submission, post-approval obligations, and marketing.