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OverviewA 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. Full Product DetailsAuthor: Joy Frestedt (President and CEO, Frestedt Incorporated, St. Louis Park, MN, USA)Publisher: Elsevier Science Publishing Co Inc Imprint: Academic Press Inc Weight: 0.450kg ISBN: 9780443220630ISBN 10: 0443220638 Pages: 576 Publication Date: 24 September 2024 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: Manufactured on demand  We will order this item for you from a manufactured on demand supplier. Table of Contents1. 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 TermsReviewsAuthor InformationJoy 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. Tab Content 6Author Website:Countries AvailableAll regions |
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