Regulatory Affairs Associate – Medical Device Italy
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Resourcing Life Science
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What to Expect Conduct regulatory impact assessments for product changes, including determination of letter-to-file versus submission requirements. Manage annual registrations, license renewals, and ongoing regulatory notifications. Support the preparation, submission, and maintenance of FDA dossiers and related technical documentation. Coordinate the collection, review, and consolidation of data... |
Vedi stipendio e Altri dettagli |
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5 giorni fa
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