Frances Richmond - Risk Assessment and Management Tools - Part 1 from fda definition of medical device complaint Watch Video
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⏲ Duration: 30 min 27 sec ✓ Published: 28-Aug-2013
Description: Frances Richmond, PhDnProfessor and Director, Regulatory Science ProgramnClinical Pharmacy and Pharmaceutical Economics and PolicynnIn this second session, Dr. Frances Richmond introduces us to the concepts of Risk Assessment and Management Tools as formal processes within the Regulatory framework we should all be aware of as clinical translational researchers who work with FDA approved drug or devices. Interestingly, she comments that these important regulatory strategies are “not particularl
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