{"title":"商业化成功的生物医学技术:药物,诊断和设备开发的基本原则(S.S. Mehta;2008)[书评]","authors":"P. King","doi":"10.1109/MEMB.2009.931786","DOIUrl":null,"url":null,"abstract":"This textbook is a nicely laid out logical road map to the development of drugs, devices, and diagnostics in the United States. Some of the topics covered include: an overview of the industry; market research; intellectual property law as practiced in the United States; new product development; an overview of Title 21 Code of Federal Regulations and the Food and Drug Administration operations; manufacturing; marketing and sales; and product liability. Each chapter begins with a bullet listing of the learning points involved in the chapter. Each chapter concludes with an overall summary, exercises as appropriate, a reference listing, and appendices as necessary. The book is a well-written introduction to the field of drug and device development and commercialization in the United States.","PeriodicalId":50391,"journal":{"name":"IEEE Engineering in Medicine and Biology Magazine","volume":"28 1","pages":"92-93"},"PeriodicalIF":0.0000,"publicationDate":"2009-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1109/MEMB.2009.931786","citationCount":"0","resultStr":"{\"title\":\"Commercializing Successful Biomedical Technologies: Basic Principles in the Development of Drugs, Diagnostics, and Devices (S.S. Mehta; 2008) [Book Review]\",\"authors\":\"P. King\",\"doi\":\"10.1109/MEMB.2009.931786\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This textbook is a nicely laid out logical road map to the development of drugs, devices, and diagnostics in the United States. Some of the topics covered include: an overview of the industry; market research; intellectual property law as practiced in the United States; new product development; an overview of Title 21 Code of Federal Regulations and the Food and Drug Administration operations; manufacturing; marketing and sales; and product liability. Each chapter begins with a bullet listing of the learning points involved in the chapter. Each chapter concludes with an overall summary, exercises as appropriate, a reference listing, and appendices as necessary. The book is a well-written introduction to the field of drug and device development and commercialization in the United States.\",\"PeriodicalId\":50391,\"journal\":{\"name\":\"IEEE Engineering in Medicine and Biology Magazine\",\"volume\":\"28 1\",\"pages\":\"92-93\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-04-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1109/MEMB.2009.931786\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IEEE Engineering in Medicine and Biology Magazine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/MEMB.2009.931786\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Engineering in Medicine and Biology Magazine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/MEMB.2009.931786","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Commercializing Successful Biomedical Technologies: Basic Principles in the Development of Drugs, Diagnostics, and Devices (S.S. Mehta; 2008) [Book Review]
This textbook is a nicely laid out logical road map to the development of drugs, devices, and diagnostics in the United States. Some of the topics covered include: an overview of the industry; market research; intellectual property law as practiced in the United States; new product development; an overview of Title 21 Code of Federal Regulations and the Food and Drug Administration operations; manufacturing; marketing and sales; and product liability. Each chapter begins with a bullet listing of the learning points involved in the chapter. Each chapter concludes with an overall summary, exercises as appropriate, a reference listing, and appendices as necessary. The book is a well-written introduction to the field of drug and device development and commercialization in the United States.