Updated for 2012 you will naturally have requirements for (non FDA) requirements. So firms have two quality systems: one for the FDA and one for the rest of the world. Personally I find this ridiculous, if not wasteful. Managing one set ofanbsp;...
|Title||:||The Key to Preventing FDA Warning Letters and 483 Observations|
|Author||:||Medical Device School|
|Publisher||:||Medical Device School -|