Zdrowie i gospodarka · 12.06.2008
Draft Guidance for Industry on Providing Regulatory Submissions in Electronic Format-Postmarketing Individual Case Safety Reports; Availability
The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled "Providing Regulatory Submissions in Electronic Format--Postmarketing Individual Case Safety Reports." This draft guidance consolidates and revises information in two existing draft guidances pertaining to electronic submission of postmarketing individual case safety reports (ICSRs) and attachments to ICSRs (ICSR attachments). The submission of ICSRs and ICSR attachments in an electronic format significantly improves the agency's efficiency in processing, archiving, and reviewing the reports.