DocumentCode :
3290074
Title :
Design control regulation
Author :
Wong, Norman
Author_Institution :
US Food & Drug Adm., Bothell, WA, USA
fYear :
1996
fDate :
4-6 Nov 1996
Firstpage :
244
Lastpage :
246
Abstract :
The Food and Drug Administration will be implementing the new GMPs for Medical Devices in June 1997. One of the significant addition to the New GMPs for Medical Devices with be part 830.30 Design Controls. Since 1984, the agency has recognized the lack of Design Controls as a significant cause for device recalls. Product design is the foundation for product development and if there is a failure in the product foundation, the product can not satisfy its intended application. It is concluded that Design Control has a significant impact on the ultimate success or failure of a new product. The value added by a manufacturer dedicating greater attention to the front end design of a new product is the less likely occurrence of unanticipated problems resulting in device recalls
Keywords :
biocontrol; biomedical equipment; product development; design control regulation; device recalls; medical devices; part 830.30 Design Controls; product development; product failure; product foundation; product success; unanticipated problems; Concurrent engineering; Drugs; Industrial control; Industrial training; Lakes; Manufacturing industries; Process design; Product design; Product development; Publishing;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Northcon/96
Conference_Location :
Seattle, WA
Print_ISBN :
0-7803-3277-6
Type :
conf
DOI :
10.1109/NORTHC.1996.564900
Filename :
564900
Link To Document :
بازگشت