Regulatory Affairs - Medical Devices
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Walters People
Bilbao
Draft and prepare product technical documentation for CE marking activities and notified body interaction to accomplish EU MDR product authorization - Understand and interpret EU and US medical device regulatory requirements - Develop regulatory strategies and plans for submissions for international product registrations - Draft and prepare 510(k) submissions and lead process through... |
Ver sueldo y Detalles |
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hace 10 horas
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