This book provides a comprehensive overview of FDA (Federal Drug
Administration) procedures. It simplifies the complexities involved
in getting FDA clearance by using an integrated approach of
clinical, engineering, and business aspects. It includes both
medical devices and drug development. This involves understanding
the structure of the FDA, its purpose, and its initiatives. This
book also examines what is needed for designing clinical trials and
addressing recalls and failures. It uses case studies to further
illustrate the integrated method stressed throughout this work.
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