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.
Your virtual conference chairperson is Ginette Collazzo, Ph.D., an authority on industrial/organizational psychology boasting more than 10 years’ experience with major drugmakers, including Bristol-Myers Squibb, J&J, Schering-Plough and Wyeth.
Audio CD/Transcript - July 26, 2012
The Audio CD/Transcript will be shipped the week of Aug. 20, 2012.