All Tools & Templates
The following is a comprehensive list of tools and templates that may be helpful for planning and conducting clinical research. For tools and templates that are tailored according to the type of study and stage of research, visit the Stages of Conducting Clinical Research.
Q
Summarizes results of site-level QM efforts and provides a framework for reporting results of QM activities.
R
Provides a template for organization of study-specific safety reporting requirements and a sample table for reference.
S
Provides definitions of important safety terminology for educational purposes. Terminology may also be used for protocol development.
For reporting Serious Adverse Events (SAEs) to NIDCR's Clinical Research Operations and Management Support (CROMS) contractor.
Provides item-by-item instructions for completing the Serious Adverse Event (SAE) Form.
Checklist to clarify the items required prior to scheduling a site close-out visit for an NIDCR-supported study.
Describes topics, tasks, and operations that are discussed during a site initiation meeting to ensure all staff, facilities, and procedures are in place to conduct the clinical research study.
Used to list subjects screened; includes those who fail screening and those who are enrolled.
Used to develop a Standard Operating Procedure (SOP). Provides standard formatting and sample section headings that can be customized.
Excel file tool that provides a framework for start-up timelines based on average durations for common components of site activation.