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. Author manuscript; available in PMC: 2021 Jul 13.
Published in final edited form as: Contemp Clin Trials. 2019 Dec 24;89:105918. doi: 10.1016/j.cct.2019.105918
Recommendation Investigators / Delegates Sponsors CROs
Move away from repetitive GCP training as the one-size-fits-all approach to qualifying investigators and their delegates for the conduct of clinical trials.
Develop educational programming that is tailored to your protocol and the members of your site team.
Recognize that completion of GCP training alone is insufficient to fully prepare for the conduct of a quality clinical trial.
Evaluate the site team’s preparedness to conduct clinical research before seeking selection as a trial site. To support the recommendations and guide this assessment, CTTI has developed a framework of characteristics describing attributes that are can be modified through learning and training [15] (Figure 1).