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.
S
Helps the investigator and research team plan orderly closure of study documents, data, and publication.
T
Identifies who on the clinical research team is responsible for completing or managing specific tasks.
Documents study-specific training completed by staff, exhibiting their qualifications to perform tasks involved in the clinical research study. Other training may also be listed on this log.
U
For reporting Unanticipated Problems (UPs) to NIDCR's Clinical Research Operations and Management Support (CROMS) contractor.
Provides item-by-item instructions for completing the UP Form.
V
Provides guidance for consistent document versioning of clinical research documents (e.g., protocol, consent document, case report forms, Manual of Procedures).