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Other CFPs
- Device Master Record & Device History Record ? requirements, contents and implementation
- Introduction to ISO 13485 Quality Management System for Medical Devices
- CE Marking: Obtaining and Maintaining EU Compliance Under the Medical Device Directive
- Full Day Virtual Seminar : Process Validation for Medical Devices - FDA Inspectors are Checking ? Are You Prepared?
- Special Issue of the JWCN on Ubiquitous Media
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