Federal Register Notice: FDA is making available a draft revised guidance for industry and reviewers, SPL Standard for Content of Labeling Technical Qs & As. It is intended to assist sponsors who submit the content of their product labeling to CDER and CBER using the Structured Product Labeling standard (SPL) in extensible markup language (XML). It also provides information to CDER and CBER staff who review and manage that product information using electronic systems. The revisions reflect technological changes and changes resulting from the requirement in the Food and Drug Administration Amendments Act of 2007 to submit drug establishment registration and drug listing information electronically. To view this notice, click here.