Grey Ra

Medical Device · 1 Employees
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About
Hands-on regulatory affairs support for small and large medical device manufacturers - Technical file management (CE, FDA, ...) - Risk management (ISO14971) - Quality System Implementation (ISO13485, FDA) - Interim Quality and Regulatory Management - Interim Project Management
Year Founded
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Medical Device
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andywarhol@greyra.nl
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awarhol@greyra.nl
first + last_initial
andyw@greyra.nl
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andy@greyra.nl
last
warhol@greyra.nl
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