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The Combination Products Handbook: A Practical Guide for Combination Products and Other Combined Use Systems
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The Combination Products Handbook: A Practical Guide for Combination Products and Other Combined Use Systems
614Hardcover
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Overview
This handbook:
- Brings clarity of understanding for global combination products guidance and regulations
- Reviews the current state-of-the-art considerations and best practices spanning the combination product lifecycle, pre-market through post-market
- Reviews medical product classification and assignment issues faced by global regulatory authorities and industry
The editor is a recognized international Combination Products and Medical Device expert with over 35 years of industry experience and has an outstanding team of contributors. Endorsed by AAMI – Association for the Advancement of Medical Instrumentation.
Product Details
ISBN-13: | 9781032291628 |
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Publisher: | CRC Press |
Publication date: | 05/16/2023 |
Pages: | 614 |
Product dimensions: | 7.00(w) x 10.00(h) x (d) |
About the Author
Susan retired from Johnson & Johnson, where her distinguished 26+ year-career included integral leadership roles in R&D, Quality Engineering, Design-to-Value, and Quality Systems Management, spanning pharmaceuticals/biotech, medical devices, and consumer health sectors, as well as strategic leadership at J&J corporate level. She served as Chair of J&J’s Design Council, advancing world-class practices in product and process design and development to drive robust, customer-centric health care solutions across J&J. She also led J&J's cross-sector Combination Products Community of Practice. Among several achievements, Susan led the team that defined and implemented the globally integrated business model to meet Combination Products health authority regulations for Janssen, J&J’s Pharmaceutical sector, and was awarded the Johnson Medal for excellence in Research and Development.
Susan also served as Executive Director and Head of Combination Products, Medical Devices, Digital Health & IVD Regulatory Affairs at Amgen, providing strategic leadership in global combination products/ device regulatory development and portfolio/project management from initial clinical investigation through registration and commercial lifecycle. She was as an advisor for internal regulatory policy priorities, health authority engagement and submissions approaches through strategic engagement and mentoring of colleagues for individual projects and portfolio. She led interactions with multiple global health authorities, and served as a catalyst for external consortium deliverables and strategic direction.
Table of Contents
Chapter 1 IntroductionChapter 2 What is a Combination Product?
Chapter 3 Regulatory Strategies
Chapter 4 cGMPs
Chapter 5 Integrated Development
Chapter 6 Risk Management
Chapter 7 Human Factors Engineering in the Design, Development and Lifecycle of Combination Products
Chapter 8 Lifecycle Management: Design Transfer through Post Market
Chapter 9
- 9A. Best Practices and Considerations for Combination Products Inspection Readiness
- 9B. US Combination Product Inspections
Part 2: Special Topics
Chapter 10 Supplier Quality Considerations
Chapter 11 Analytical Testing Considerations
Chapter 12 Biological Products Considerations
Chapter 13 Connected Health
Chapter 14 Evolving Global Regulatory Landscape