This webinar will provide practical tips to the clinical research site staff in developing a process for obtaining Informed Consent. It will show how you can assure the subject fully understands the clinical research study. You will also learn about the appropriate documentation for the consenting process.
Why Should You Attend:
The International Conference on Harmonization Good Clinical Practice Guidelines (ICH GCP) requires that all research sites have a process for informing subjects about the clinical research study the subject is considering participating in. Many clinical research sites, from the small office set-up to large academic institutions, are not aware of the process required in obtaining informed consent.
This webinar will instruct the attendees on the requirements outlined in ICH GCP and how to document the consenting process in the subject’s source documentation. It will assist healthcare professionals in obtaining ethical consent from their potential subjects that not only protects the rights of subjects but will pass Regulatory Agencies audits.
Added by complianceonlinecom on January 10, 2013