Code of Federal Regulations 21 : Title 21, Food and Drugs, Parts 800 to 1299 Revised as of April 1 2004

This section of the Code of Federal Regulations contains the current good manufacturing practice regulations for medical devices that have been revised and incorporated into quality system regulations for medical devices and especially pertains to blood bank computer systems.Office of the Federal Register National Archives and Records Administration is the author of 'Code of Federal Regulations 21 : Title 21, Food and Drugs, Parts 800 to 1299 Revised as of April 1 2004', published 2004 under ISBN 9783805578943 and ISBN 3805578946.