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Premarket Approvals (PMAs)
September 16, 2015, FDLI/CDRH In-House Training: Introduction to Medical Device Law and Regulation Workshop
Postmarking Issues
November 3, 2016, FDLI Introduction to Medical Device Law and Regulation Course
Dealing with Adverse Events/Product Problems
June 13-14, 2016, FDLI/CDRH In-House Training: Introduction to Medical Device Law and Regulation Workshop
Postmarket Issues And Strategies
March 31, 2016, FDLI Hot Topics in Medical Device Law Conference