Conducting Clinical Trials in Resource-Limited Settings
25 - 26 August 2011
Training course
San Francisco, CA, US
Any pharmaceutical manufacturer conducting trials in resource-limited settings has to deliver fair and practicable solutions. Sensitivity to cultural differences is key when interacting with local investigators, authorities, monitors, and study participants. Good local knowledge is needed to navigate the challenges of the regulatory landscape. Particularly in Africa, capacities and infrastructure must often be strengthened, and many achievements taken for granted in the Western research world may pose barriers in resource-limited settings
Organiser: Barnett International