On the evening of May 30th, you are again reviewing a Novartis POP and identify a record from a participant from May 25th where the record mentioned an AE associated with the use/ mention of a Novartis product. You fill in the AE form and fax it to Novartis the next morning when you are back in the office. What is the "Manufacturer Receipt Date" of the AE?

Answer rating: 100% (QA)

The Manufacturer Receipt Date of the Adverse Event AE associated with t... View the full answer