Our Team
The company is led by Julie Moore with a growing team of highly experienced consultants. Our Associate Consultants each have over 15 years regulatory experience working in the medical device industry. Collectively we have experience of working with global regulations in a range of medical devices and cover all areas of pre and post market regulatory affairs, clinical affairs and quality management system expertise.
Julie Moore
Managing Director
A highly experienced medical device regulatory consultant and coach, Julie helps businesses with global strategic and executional compliance challenges.
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James Allard
Associate Consultant
Results-driven and committed, James has over 18 years of industry experience in Quality, Regulatory, Design Assurance and Device Development.
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Maria Carrasco Duguine
Associate Consultant
With two decades of dedicated experience in the regulatory field, Maria brings a wealth of knowledge and expertise to the table as a seasoned Chemist.
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Chris Hands
Associate Consultant
A seasoned clinical evaluation professional, with 15 years experience, Chris possesses a wealth of knowledge in this field.
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Associate Consultant
Valerie is a highly experienced and results-oriented US based regulatory affairs manager, specializing in medical device products.
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Katy Evans
Business Operations Director
A qualified accountant, with expertise in programme design and implementation. Katy is responsible for overall operations and performance of the company.
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