Regulatory Support

Regulatory Support
Product Description

Armed with decades of experience and a mature Quality System, we collaborate with you to ensure your medical device is market-ready and complies to all latest industry regulations.

Our capabilities and experience include: 
- Fully integrated Quality System- Diversified & approved international suppliers
- ISO 13485 Medical Devices Quality Management
- ISO 14971 Risk Management for Medical Devices
- CE Mark certification
- FDA 21 CFR 820 compliant
- Device History File
- Device Master Records
- Device History Record

Duoject Medical Systems Inc

  • CA
  • 2020
    On CPHI since
Specifications

Duoject Medical Systems Inc

  • CA
  • 2020
    On CPHI since

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