Constantina Kinni

Regulatory Affairs Practice – Europe

OVERVIEW

FOCUS AREAS

Regulatory Affairs expert with 12+ years in CMC, specializing in global pharmaceutical submissions for Chemicals and Biologics.

CMC authoring and submissions

Developing regulatory strategies

Change control assessment and management

Regulatory intelligence

As CMC (Chemistry, Manufacturing and Controls) Manager of ELIQUENT Life Sciences, Constantina Kinni is working alongside a diverse array of clients on various projects covering pre- and post-approval submissions for Chemicals and Biologics. Her ability to manage intricate regulatory requirements underscores her commitment to the industry’s highest standards.

Constantina’s professional journey encompasses a 13-year tenure in Regulatory Affairs, with a particular focus on CMC; authoring quality sections submissions, developing and implementing regulatory CMC strategies, providing regulatory expertise on cross-functional project teams and managing complex project activities across multiple teams and departments. Her involvement in CMC projects equipped her with the ability to adeptly manage the intricate regulatory frameworks that govern this sector. Constantina’s capabilities are specifically tailored to meet the stringent requirements of the pharmaceutical regulatory field, positioning her as an important contributor to any team striving for excellence within this challenging industry.

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