Every month you get a comprehensive briefing on the latest
regulatory developments around the world, including the U.S., Europe,
Latin America, Asia, Canada, Australia and more. Plus you get actual
full, official English-language texts of important, hard-to-obtain
proposals, regulations, rules, directives, guidances and other
documents to keep you completely up-to-date on significant developments
in medical device regulatory policies worldwide. Save hours on research
time and overcome barriers to application approval.