Join us for a stimulating presentation that analyzes the laws, regulations, policies and trends intended mostly for healthcare operations that are unintentionally (or intentionally) bleeding over into research operations. While sites and sponsors have many opportunities to hear what the FDA, NIH and OHRP are doing, these activities often come as a surprise as they are not generally part of the clinical trials ecosystem that they affect.
Recall the relevant portions of the varying laws and regulations related to current U.S. healthcare reform
Analyze the potential impact of the laws and regulations on the research industry
Interpret how the laws and accompanying regulations affect them