Wiliam Tillett

Regulatory Affairs Practice – Europe

OVERVIEW

FOCUS AREAS

Several years experience in regulatory and quality teams within the private pharmaceutical and government agency industries.

Regulatory Affairs and strategy
Project management
Data analysis
Submitting critical regulatory documentation

Knowledgeable in the Regulatory and Quality space, William has 4 years’ experience in a Regulatory and Quality team, in both the Department of Health and UK Health Security Agency. Hands on experience with medical device project management and Quality Management Systems. Always keen to learn, with a particular interest in Neuroscience after studying the subject at the University of Nottingham. William’s strengths lie in his effective interactions via strong communication skills, enthusiasm and teamworking capabilities.

William is utilizing his extensive prior experience with medical device supplier management for the UK government, as well as handing requests from the MHRA, to ensure that any client he is responsible for will always have a great relationship with Eliquent. As an extremely enthusiastic and hardworking individual, William will throw himself into any project or opportunity to further his exposure to widen his knowledge and capabilities. Holds strong analytic and data transformation skills for large datasets, and innovative ability for making standardized dashboards. William has experience leading and running medical device projects to meet quality standards, which have proven very useful to help solve any regulatory problems or tough projects that Eliquent are presented with.

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