Applied biomaterials standards report.

Abstract

The purpose of my column is to provide readers with current information on biomaterials-related standards produced by both private groups and government agencies, and standards-related activities. Standards are descriptive documents given official status by their producers and, in the case of biomaterials, they are generally intended to provide formalized descriptions of (a) materials used in the construction of medical devices, (b) materials used directly in surgical repairs, (c) test methods to evaluate materials for such applications, and (d) methods for handling or processing such materials. Please consider this column not only a place to obtain biomaterials standards information but also a place to submit news of biomaterials standards developments in order to get the information before the public. This invitation extends to all members of any and all professional organizations and government agencies in the United States and abroad who are active in standards development and would like specific activities or standards publicized. I will present the information in this column to the extent that allotted space allows. And last, a caveat--since this is a column, it contains both factual information and opinions. I will make every effort to make it clear which is which. Also, as a frame of reference, please note that this column was written and submitted in January, 1989.