How to Manage Multiple Site Trials while Ensuring Consistency of Study Conduct
Interview with Sophie Biguenet, Medical Director, Global Clinical Research Virology at Bristol-Myers Squibb
Due to the increasing pressure from global regulatory authorities to successfully implement regulations and ethical standards into pediatric study processes, companies must ensure that their clinical programmes are on par with global standards. Journal for Clinical Studies and Marcus Evans, organisers of the 9th Annual Pediatric Clinical Trials Conference, speak with Sophie Biguenet, Medical Director, Global Clinical Research Virology at Bristol- Myers Squibb on how to close the gap between regulatory requirements, study development and execution of trials.
http://jforcs.com/jcs/wp-content/uploads/2013/04/How-to-Manage-Multiple-Site-Trials-while-Ensuring-Consistency-of-Study-Conduct.pdf