Stay on top of key changes in pharmaceutical regulation around the
world with this monthly resource for rules and standards flowing from
the FDA, the European Agency for the Evaluation of Medicinal Products,
Health Canada, Australia's TGA, the International Conference on
Harmonization and other agencies in Europe, Japan and elsewhere. In
addition to a comprehensive briefing, you get actual, full official
English-language texts of important, hard-to-obtain proposals,
regulations, rules, directives, guidances and other documents, to help
you prepare better-documented, properly formatted drug applications for
fastest processing.
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