Overview
This virtual live training course will provide participants with high level real world, actionable information on the content and development of global regulatory strategies.
The three afternoon sessions will include expert advice on drug development and initial approval in the major regions, as well as the information needed to develop regulatory strategies for other key and emerging markets around the world.
Descriptions of local regulatory environments required for drug approval in key markets will be enhanced by case examples. Particular focus will be on the EU, US, Japan, as well as key markets in Asia, Latin America, Africa and the Middle East. The course will also discuss topics across the regions with off-spring in the EU and US regulatory environment, along with overviews of emerging trends and the ever changing regulatory environment in the selected regions.
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