Capturing the growth of the global medical device market in recent years, this practical new guide is essential for all who are responsible for ensuring safety in the use and manufacture of medical devices. It has been extensively updated to reflect significant advances, incorporating combination products and helpful case examples of current real-life problems in the field. The Third Edition explores these key current trends: global device markets continually advancing technology the increasing harmonization of device safety regulation worldwide Each aspect of safety evaluation is considered in terms of International Standards Organization (ISO), US Food and Drug Administration (FDA), European Union (EU), and Japanese Ministry of Health and Welfare (MHW) perspectives. In addition, the book reflects the role of the continuing growth of technology in the incorporation of science, particularly in the areas of immunotoxicology and toxicokinetics.Laskin, D.L., Laskin, J.D., Weinstein, I.B., and Carchman, R.A. (1981). Induction of ... Selected aspects of cell and molecular biology of in vivo ... 209a223. Marzulli, F.N. and Maibach, H.L. (1996). ... Prepared for the Consumer Product Safety Commission, National Academy of Sciences, Washington, D.C., pp. 36a39.
|Title||:||Safety Evaluation in the Development of Medical Devices and Combination Products, Third Edition|
|Author||:||Shayne C. Gad, Marian G. McCord|
|Publisher||:||CRC Press - 2008-10-20|