Join us for the first-of-its-kind workshop on building in and implementing quality in modern clinical investigations from the inception of the research through its completion.

As clinical investigations become more complex and global, FDA must continue to evolve and modernize the oversight and monitoring of research. In June 2006, FDA announced the BIMO Initiative, which specifically addresses concerns surrounding the protection of human subjects and the integrity of data in clinical trials (www.fda.gov/bbs/ topics/NEWS/2006/NEW01396.html).

FDA continues to seek input from clinical researchers and all other relevant parties on the challenges of and potential solutions for the establishment of an integrated approach to protecting human subjects.

HIGHLIGHTS
•FDA speakers from CBER, CDER, CDRH, CVM, OC, AND ORA
•Featured speakers/panelists from Academia, AAMC, ACRO, ADVAMED, BIO, CDISC, Data Quality Research Institute, MHRA, NIH, AND PhRMA.