The FDA categorizes medical devices into three classes, namely Class I, Class II, and Class III. Regulatory control increases from Class I to Class III. 1 The agency has classified approximately ...
Sevilla said that as early as 2020, the agency had already made issuances to guide stakeholders and consumers on the classification of medical devices. The task force will help in solving the ...
The UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) has launched a consultation period calling on the public ...