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Planning, Writing and Reviewing Medical Device Clinical Performance Evaluation Reports (CERs/PERs): A Practical Guide for the European Union Other Countries
Barnes and Noble
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Planning, Writing and Reviewing Medical Device Clinical Performance Evaluation Reports (CERs/PERs): A Practical Guide for the European Union Other Countries in Franklin, TN
Current price: $150.00
Barnes and Noble
Planning, Writing and Reviewing Medical Device Clinical Performance Evaluation Reports (CERs/PERs): A Practical Guide for the European Union Other Countries in Franklin, TN
Current price: $150.00
Loading Inventory...
Size: Paperback
A Practical Guide to Planning, Writing, and Reviewing Medical Device Clinical Evaluation Reports
guides readers through clinical data evaluation of medical devices that is in compliance with the EU MDR requirements and other similar regulatory requirements throughout the world. This book brings together knowledge learned as the author constructed hundreds of CERs and taught thousands of learners on how to conduct clinical data evaluations. This book will support training for clinical engineers, clinical evaluation scientists, and experts reviewing medical device CERs, and will help individual writers, teams and companies to develop stronger, more robust CERs.
guides readers through clinical data evaluation of medical devices that is in compliance with the EU MDR requirements and other similar regulatory requirements throughout the world. This book brings together knowledge learned as the author constructed hundreds of CERs and taught thousands of learners on how to conduct clinical data evaluations. This book will support training for clinical engineers, clinical evaluation scientists, and experts reviewing medical device CERs, and will help individual writers, teams and companies to develop stronger, more robust CERs.
A Practical Guide to Planning, Writing, and Reviewing Medical Device Clinical Evaluation Reports
guides readers through clinical data evaluation of medical devices that is in compliance with the EU MDR requirements and other similar regulatory requirements throughout the world. This book brings together knowledge learned as the author constructed hundreds of CERs and taught thousands of learners on how to conduct clinical data evaluations. This book will support training for clinical engineers, clinical evaluation scientists, and experts reviewing medical device CERs, and will help individual writers, teams and companies to develop stronger, more robust CERs.
guides readers through clinical data evaluation of medical devices that is in compliance with the EU MDR requirements and other similar regulatory requirements throughout the world. This book brings together knowledge learned as the author constructed hundreds of CERs and taught thousands of learners on how to conduct clinical data evaluations. This book will support training for clinical engineers, clinical evaluation scientists, and experts reviewing medical device CERs, and will help individual writers, teams and companies to develop stronger, more robust CERs.
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