Specialist, Regulatory Affairs

marketed products; documents including, but not limited to: Significant Risk Determination Requests (SRDs); IDE...) including writing and submitting pre-sub, IDE application and/or PMA documents to FDA CDRH Professional and/or academic...

Lugar: Boston, MA | 31/10/2024 01:10:13 AM | Salario: S/. No Especificado | Empresa: Foundation Medicine