Working in pharmaceutical industry, sooner or later you will be interacting with European regulatory authorities. There are many opportunities along your drug' development lifecycle for you to bring your message to regulators. In addition, environmental turbulence or major regulatory changes may affect your programme and you will need to make informed decisions.

To ensure you receive meaningful and useful advice, it’s important to be fully prepared and have a strategy in place.

Register to this webinar and find out whether you’re making the most of all these opportunities to facilitate and optimise your drug development program.

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The Presenter

Dr Roz Cox

Principal Consultant

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