Anna Conte
Regulatory Submission Manager at Fortrea
Based in Italy
7-day free trial · no credit card
Seniority
Manager
Department
Legal
Location
Italy
Industry
Biotechnology Research
Company size
11K
Contact information
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a•••••••@fortrea.com
Phone
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Background
About Anna Conte
More thank 25 years experience in the clinical trials II-IV Phases, as CRA; LCRA; PM and Clinical Operation Specialist, specialised in the Start Up activities and finally in the Global Regulatory Affairs activities. Actually accountable for global submissions to any RA/EC and third bodies. Coordinating the local regulatory team for ensuring all timely submissions of appropriate documentation to RA globally. Responsible for providing regulatory consultancy advice to client companies and to internal project team.
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