Medical device regulatory practices : an international perspective / Val Theisz.
By: Theisz, Val [author.]
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Material type: ![materialTypeLabel](/opac-tmpl/lib/famfamfam/BK.png)
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Contents:
1. Overview of the international regulatory framework for medical devices -- 2. Safety and effectiveness -- 3. Technical documentation -- 4. Pre-market phase -- 5. Regulatory submissions, approvals and registrations -- 6. Post-market phase.
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1. Overview of the international regulatory framework for medical devices -- 2. Safety and effectiveness -- 3. Technical documentation -- 4. Pre-market phase -- 5. Regulatory submissions, approvals and registrations -- 6. Post-market phase.
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