The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing.
Roxane Laboratories, Inc., announced that it is conducting a nationwide voluntary
recall of a single manufacturing lot of Azathioprine tablets, USP 50 mg, (NDC
00054-4084-25, Lot 558470A, Exp Mar 2009). Azathioprine is used to help prevent
rejection in kidney transplant patients, and can also be used to manage severe