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  3. Erica Giordano

As an Associate Director, Erica is responsible for assisting in the preparation and compilation of high-quality US and EU regulatory submissions for drugs and biologics, and liaising with clients for FDA, EMA, and MHRA interactions, meetings and correspondence. She provides strategic and regulatory input on the development of these products, working closely with clients on a long term basis and elaborating roadmaps covering US, EU and UK.

Insights by Erica Giordano