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.Within the CDRH there is a range of groups (called divisions) that focus on specific areas of use for devices (e.g., general and restorative devices; ... Regulatory Requirements for Medical Devices: A Workshop Manual. ... Gad, S.C. (2001).
|Title||:||Safety Evaluation of Medical Devices|
|Author||:||Shayne C. Gad|
|Publisher||:||CRC Press - 2001-12-04|