Sites are so busy that quality assurance is often overlooked and only becomes a focus when issues arise or when there is an audit. Our easy to implement techniques include quality assurance checks, office guidelines, checklists, and lessons learned.
Find out more »Thanking and returning results to study participants honors research volunteers, helps build trust in the clinical research process, and is simply the right thing to do! Join us for an engaging discussion on the benefits, methodology, and resources available to develop thank you cards and lay summaries of aggregate results in a language and format that is understandable and easy to read.
Find out more »Join us in reviewing ICH E8. Learn to describe internationally accepted principles and practices for the conduct of clinical trials and overall development strategy, facilitate the evaluation and acceptance of international trial data, and present an overview of other ICH guidelines pertinent to clinical trials.
Find out more »When conducting concurrent studies with limited resources it can be difficult to ensure quality and timely data collection and data entry for each study. This session will provide new and current Project Managers with useful tools to streamline their workload and hopefully decrease some of the common stress of the role.
Find out more »Ensuring that your Investigator Site File (ISF) and Trial Master File (TMF) are built in a way that the complete documentation tells the story of the study, will ensure that you are ready come inspection day. The session will also include common GCP violations that are evident in the TMF/ISF and can result in findings.
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