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Series and Certificate Programs / QA•RA Professional Institute / For Medical Device Professionals
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Medical Device Leadership Certificate. Request Courses in Your Area. VIEW CART ( 0. Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification. Series and Certification Programs. Advanced Post-Market Surveillance Series. Part 1: Post-Market Surveillance Function – Manage it efficiently and effectively. Part 2: Harmonizing Post-Market Surveillance Processes. Design Controls Series Certificate Program. The FDA Safety and Innovatio...
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VIEW CART ( 0. Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification.
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On-Campus Courses / QA•RA Professional Institute / For Medical Device Professionals
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Medical Device Leadership Certificate. Request Courses in Your Area. VIEW CART ( 0. Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification.
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Medical Device Leadership Certificate. Request Courses in Your Area. VIEW CART ( 0. Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification.
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Medical Device Leadership Certificate. Request Courses in Your Area. VIEW CART ( 0. Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification. FDA and Legislation for Medical Devices. FDA Report: Strengthening our National System for Medical Device Postmarket Surveillance (September 2012). FDA Safety and Innovation Act (FDASIA) July 2012. FDA Global Engagement Report (April 2012). FDA website – Main page. Health Canada Medical ...
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VIEW CART ( 0. Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification. We're sorry, currently no items were found in your cart. Please select from the available courses.
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FDASIA Series / QA•RA Professional Institute / For Medical Device Professionals
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VIEW CART ( 0. Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification. Download Summary of FDASIA Series. Jim O 'Reilly, JD. NOTE: The FDA has created FDASIA Track on their website. In order to track progress on guidances and reports required by FDASIA over the next four years. Or, we have provided a pdf version of the device-relevant actions here:. Download FDASIA Track for Devices pdf. The Unique Device Identifier system.
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Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification.
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MDR Series / QA•RA Professional Institute / For Medical Device Professionals
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VIEW CART ( 0. Design Controls Series Certificate Program. Advanced Post-Market Surveillance Series. How to Implement the Unique Device Identification. Download Summary of MDR Series. What Is The Challenge? As a medical device manufacturer, you are aware that this topic is critical to master, since as an involved company you must establish a decision tree for determining risk to patient safety and potential product recall. Here’s The Solution:. Three Categories are established for this series:. One webin...
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