Transparency is a key component in the conduct of clinical trials. Laws and regulations related to posting clinical trials and study results to public registries continue to change. There is an expectation that clinical trial information will be placed in the public domain for patients, their families, and physicians, researchers and healthcare providers to access. This session will focus on the requirements and responsibilities of sponsors, CROs, investigators and clinical sites regarding posting clinical trials and study results on public clinical trial registries/data banks.
Describe the differences between patient registries and clinical trial registries/data banks
Identify the laws and requirements related to clinical trial disclosure for your clinical trial
Determine responsibilities of the Sponsor, CRO, Principal Investigator and Clinical Site with regard to posting clinical trials