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Executive Briefing Series (formerly The Food & Drug Letter)
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//www.fdanews.com/ext/resources/files/The_Food_And_Drug_Letter/2016/Avoiding-Data-Integrity-Breaches-ExecSeries.pdf?1458769829
March 23, 2016
//www.fdanews.com/ext/resources/files/The_Food_And_Drug_Letter/2016/Aging-Aseptic-and-Biologic-Manufacturing-Sites-ExecSeries.pdf?1455904051
February 19, 2016
//www.fdanews.com/ext/resources/files/The_Food_And_Drug_Letter/2016/Managing-HCT_Ps-Under-the-FDAs-New-Guidelines-ExecSeries.pdf?1452729390
January 13, 2016
//www.fdanews.com/ext/resources/files/The_Food_And_Drug_Letter/2015/Drugmakers-Guide-to-Global-Quality-API-Manufacturing-ExecSeries.pdf?1447282202
November 6, 2015
//www.fdanews.com/ext/resources/files/The_Food_And_Drug_Letter/2015/Quality-Risk-Management-for-Pharmaceuticals-ExecSeries.pdf?1445265814
October 19, 2015
//www.fdanews.com/ext/resources/files/The_Food_And_Drug_Letter/2015/Expediting-the-FDA-Generic-Drug-Approval-Process-ExecSeries.pdf?1442239675
September 14, 2015
//www.fdanews.com/ext/resources/files/The_Food_And_Drug_Letter/2015/Understanding-EU-Drug-Safety-Reporting-ExecSeries.pdf?1439305154
August 11, 2015