Simplifying Global Compliance
Designing and Executing Observational Studies Using Registries to Collect Real World Effectiveness and Safety Data
This webinar features United BioSource’s Peggy Schrammel, an expert on outcomes research and an experienced designer of post-approval clinical trials and patient registries across multiple therapeutic areas. She’ll be your guide through the maze of new requirements, standards and rules that could spell success for your products — or failure.
Audio CD/Transcript - Dec. 14, 2010
The Audio CD/Transcript will be shipped the week of Jan. 10, 2011.
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