June 27, 2018
The design is complete. The label is finalized. The product is approved and sold. But the risks of liability don’t end there. In this webinar, Butler Snow LLP’s Kyle Cummins will discuss relevant post-sale duties and product-liability doctrines affecting manufacturers after a product is on the marke...
May 29, 2018
Two new major pieces of legislative action-- the User Fee Law (FDARA) and the 21st Century Cures Act-- will likely have serious effects on your operations. This webinar will look at how these pieces of legislation as well as CDRH's agenda in the coming years are likely to affect medical device compa...
April 25, 2018
The Department of Justice places a high priority on criminally prosecuting individuals including sales reps and executives for their corporations’ misconduct, including misconduct often at the heart of products liability lawsuits. In this webinar, Andrew Tharp of Butler Snow LLP will discuss DOJ cri...
Previously Recorded on March 21, 2018
Learn how you can leverage one of the top trends in the medical device industry, the MedAccred progr...
Previously Recorded on February 27, 2018
In an increasingly litigation-driven world, even the best of intentions (and FDA approval) in labeli...
Previously Recorded on January 24, 2018
This one-hour webinar will review and bring you up to date on: Recent FDA enforcement trends for de...
