Study Design
This short course provides an overview of clinical trials and their phases, including the intricacies of masking, randomization, cohort, and cross-sectional studies.
The purpose of this activity is to educate medical professionals on overview of clinical study design.
During this workshop, speakers will respond to specific request for applications, including both the ECHO ISPCTN Junior Investigator Pilot RFA and a broader lens towards using other RFAs to tailor grant submissions.
The purpose of this activity is to educate healthcare providers with the most up-to-date information on expanded access to investigational drugs in clinical trials.
This module provides an overview of when investigational products and devices can be used for emergencies and the steps for approval.
During this webinar, Dr. Douglas Adams discusses what a protocol is and how they differ among mechanisms.
In the webinar, speakers will discuss the guidance from the FDA to Industry on Development and Licensure of Vaccines to prevent COVID-19 regarding clinical trials and characteristics of 2 COVID-19 vaccines submitted for Emergency Use Authorization.
In this module, the speaker explains the role of a statistician in clinical trial design, defines basic statistical terms, interprets clinical study types and endpoints, and identifies important methods for statistical data analysis. *ECHO ISPCTN Core Curriculum Module
This module identifies the difference between protocol versus grant review, applies knowledge of review process to creating rigorous and competitive clinical trial protocols, and applies lessons from ECHO ISPCTN protocol chairs to future ECHO ISPCTN reviews. *ECHO ISPCTN Core Curriculum Module
This module explains the difference between Cohort, Case-control & Cross-sectional studies and Retrospective Cohort Study.
This activity covers Quality Improvement design, explains the IRB Approval process, and identifies potential outcomes.
