Courses #EU - Eventura World

Data Integrity – In Compliance with CSA, 21 CFR Part 11, SaaS/Cloud, EU GDPR

Supplier Management with the new EU MDR 745/2017

3-Hour Virtual Seminar On U.S. FDA And Eu Medical Device Directive Requirements For DHFS, DMRS, DHRS, And TF/DDS

Deconstructing the EU MDR with Principles of Lean Documents and Lean Configuration

EU's New Regulation 535/2014 On Clinical Trials - Insights Into Effective Clinical Trials

CE Marking in the EU – Latest Regulations

FDA vs EU Inspections - Differences And Similarities - How To Get Prepared