Giorgia Loddo
Associate Manager Ii, Global Regulatory Submissions Lead at Fortrea
Based in Italy
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Seniority
Other
Department
Other
Location
Italy
Industry
Biotechnology Research
Company size
10001+
Contact information
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g•••••••@fortrea.com
Phone
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Background
About Giorgia Loddo
Responsible for preparation and submission of all phases clinical trials in several therapeutic areas (including radiodrugs and GMOs), and clinical investigation with all classes medical devices under MDR in Europe and UK. Serving as EU subject matter expert in MD field for clients and internal stakeholders.
Decision-makers
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