Regulatory Affairs
Published date: 2026/11/06
- Location: Thane, Maharashtra, India
Maintain regulatory files. Maintain and update regulatory authorizations, such as IDEs, Medical device licenses, and CE dossiers for certifications etc.
· Documenting technical file for ISO 9001:2005 and Implementing compliance to performance of Medical Device
· Documenting technical file for ISO 9001:2005 and Implementing compliance to performance of Medical Device
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