Federal Register Final rule: FDA is amending its medical device regulations to implement a nomenclature change and to ensure accuracy and clarity in the agency's regulations. It replaces the phrase “good manufacturing practice regulations” with the phrase “good manufacturing practice requirements of the quality system regulation” in 21 CFR parts 860, 862, 864, 866, 868, 872, 874, 876, 878, 880, 882, 886, 888, 890, and 892. To view this final rule, click here.
