FDA relaxes UDI requirements for some Class I devices The US Food and Drug Administration (FDA) has reviewed requirements for the use of Unique Device Identifiers (UDI)
An update from the office for Product Safety and Standards – OPSS concerning statutory instrument – SI – amending: Annex II – Prohibited Substances and Annex III
The Office for Product Safety and Standards – OPSS – call for data The Office for Product Safety and Standards – OPSS have issued a ‘Call for
