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Strategies for Working with Global Regulatory Agencies

It’s never too early to start crafting a global regulatory submissions strategy.

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It’s never too early to start crafting a global regulatory submissions strategy.  Early engagement with regulatory authorities can help boost success rates and shorten clinical development timelines but there are potential pitfalls to avoid as well. Read our strategies on how to maximize benefits and minimize hazards when seeking scientific advice from the European Medicines Agency (EMA) as well as how to be smart about pre-IND meetings and other early stage FDA meetings.