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my name is laura graham im in the office of policy for pharmaceutical quality which is one of the sub offices within cders office of pharmaceutical quality or opq today im going to be talking to you about how fda has been assessing facilities during the coving 19 public health emergency when travel restrictions are in place im going to be talking about both prioritizing inspections and the use of alternate tools to assess facilities during the public health emergency im also going to talk about the impact of the phe appending and approved applications i want to be clear from the start though that while im presenting information that crosses disciplines at the fda i am by no means an expert in all of these areas however the good news is that i have experts around the agency on the panel discussion that follows my presentation who can help fill in any blanks and answer your questions so what am i specifically going to be talking about today im going to start by providing some back