Published in Hospital Law Weekly, May 24th, 2007
Growing demands from regulators for postmarket-approval data along with the need for data to support commercial markets are fueling biotech company product and disease registries. This session will guide participants through the decision-making, structuring, legal/regulatory, implementation and operational components of establishing and operating a global product/disease registry.
Topics covered will include:
Understanding when a...
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Source: Hospital Law Weekly (2007-05-24)
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