The International Council for Harmonisation (ICH) has released a draft guideline which outlines a harmonized template for clinical trial protocols to support consistent reporting among sponsors.
The draft guideline, as well as the template and specifications for the template, were endorsed by the ICH Assembly on 27 September and released for public consultation on 21 October.
The guideline aims to have clinical trial protocol templates that are “complete, free from ambiguity, well organised, and aligned with quality by design principles as set forth in other ICH guidelines.”
The guideline notes that “variability in format and core content” of clinical trial protocols “contributes to inefficiencies and difficulties in searching, reviewing, and assessing clinical trial protocols.”
Clinical trial protocols describe the processes and procedures governing the conduct of clinical trials. The guideline states that “to date, no internationally adopted harmonized standard has been established for the format and content of the clinical trial protocol to support consistency across sponsors and for the electronic exchange of protocol information.”…