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Planning, Writing and Reviewing Medical Device Clinical and Performance Evaluation Reports (CERs/PERs) A Practical Guide for the European Union and Other Countries

Frestedt Joy
Heftet / 2024 / Engelsk

Produktdetaljer

ISBN
9780443220630
Publisert
2024-09-24
Utgiver
Vendor
Academic Press Inc
Vekt
1420 gr
Høyde
276 mm
Bredde
216 mm
Aldersnivå
P, 06
Språk
Product language
Engelsk
Format
Product format
Heftet
Antall sider
576

Forfatter
Frestedt Joy

Om bidragsyterne

Joy Frestedt Is the President and CEO for Frestedt Incorporated, a consulting group of over 70 experts providing services in broad CRQE areas of clinical trial development and execution, as well as US and international regulatory compliance, management of corporate quality systems, and biomedical engineering. She has managed clinical research, regulatory affairs, and quality systems for more than 40 years and has published more than 100 manuscripts, as well as book chapters. With a PhD in Pathobiology from the University of Minnesota Medical School, her experience includes designing, conducting and overseeing clinical trials as well as negotiating regulatory submissions and developing quality systems for companies like the University of Minnesota, Orphan Medical, Astra Zeneca Pharmaceuticals, Johnson and Johnson, Medtronic, and Mayo Clinical Trial Services.

Planning, Writing and Reviewing Medical Device Clinical and Performance Evaluation Reports (CERs/PERs) A Practical Guide for the European Union and Other Countries

Frestedt Joy
Heftet / 2024 / Engelsk
Frestedt Joy
Heftet / 2024 / Engelsk
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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.
Les mer
1. Preface 2. Introduction 3. Planning Clinical Evaluations of Medical Devices 4. Writing Clinical Evaluation Reports of Medical Devices 5. Identifying clinical data 6. Appraising clinical data 7. Analyzing clinical data 8. Integrating post market surveillance systems 9. Integrating risk management systems 10. Evaluating Risk:Benefit Profiles 11. Incorporating post market clinical follow up studies 12. Writing Summaries of safety and clinical performance 13. Reviewing medical device clinical evaluation reports 14. Understanding CER Regulations outside of Europe 15. Forecasting CER future directions 16. Appendixes 17. Index and Definition of Terms
Les mer
Comprehensive guide to writing clinical evaluation reports of medical devices, in compliance with the new European Union Medical Device Regulations
Identifies and explains data analysis for clinical evaluation of medical devices Teaches readers how to understand and evaluate medical device performance and safety in the context of new regulations Provides analysis of new clinical evaluation criteria in the context of medical device design as well as in-hospital deployment and servicing
Les mer

Relaterte produkter

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.
Les mer
1. Preface 2. Introduction 3. Planning Clinical Evaluations of Medical Devices 4. Writing Clinical Evaluation Reports of Medical Devices 5. Identifying clinical data 6. Appraising clinical data 7. Analyzing clinical data 8. Integrating post market surveillance systems 9. Integrating risk management systems 10. Evaluating Risk:Benefit Profiles 11. Incorporating post market clinical follow up studies 12. Writing Summaries of safety and clinical performance 13. Reviewing medical device clinical evaluation reports 14. Understanding CER Regulations outside of Europe 15. Forecasting CER future directions 16. Appendixes 17. Index and Definition of Terms
Les mer
Comprehensive guide to writing clinical evaluation reports of medical devices, in compliance with the new European Union Medical Device Regulations
Identifies and explains data analysis for clinical evaluation of medical devices Teaches readers how to understand and evaluate medical device performance and safety in the context of new regulations Provides analysis of new clinical evaluation criteria in the context of medical device design as well as in-hospital deployment and servicing
Les mer

Produktdetaljer

ISBN
9780443220630
Publisert
2024-09-24
Utgiver
Vendor
Academic Press Inc
Vekt
1420 gr
Høyde
276 mm
Bredde
216 mm
Aldersnivå
P, 06
Språk
Product language
Engelsk
Format
Product format
Heftet
Antall sider
576

Forfatter
Frestedt Joy

Om bidragsyterne

Joy Frestedt Is the President and CEO for Frestedt Incorporated, a consulting group of over 70 experts providing services in broad CRQE areas of clinical trial development and execution, as well as US and international regulatory compliance, management of corporate quality systems, and biomedical engineering. She has managed clinical research, regulatory affairs, and quality systems for more than 40 years and has published more than 100 manuscripts, as well as book chapters. With a PhD in Pathobiology from the University of Minnesota Medical School, her experience includes designing, conducting and overseeing clinical trials as well as negotiating regulatory submissions and developing quality systems for companies like the University of Minnesota, Orphan Medical, Astra Zeneca Pharmaceuticals, Johnson and Johnson, Medtronic, and Mayo Clinical Trial Services.

Relaterte produkter