The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing.
The agency said the testimonials do not “adequately support the suggestion in the presentation that other patients switching to Livalo from other statins will experience a similar reduction in side effects.”
Home » Events » A World Apart Understanding Differences in EU and U.S. Drug and Device Adverse Event Reporting
Clear your calendar for Wed., May 30, when you’ll hear from top experts in an intensive “virtual conference,” A World Apart: Understanding Differences in EU and U.S. Drug and Device Adverse Event Reporting
Audio CD/Transcript - May 30, 2012
The Audio CD/Transcript will be shipped the week of June 25, 2012.