The study sponsors had no role in the study design, analysis or reporting.
This clinical trial infrastructure unites study sponsors with 22 academic veterinary centers to support multicenter clinical trials of investigational therapeutics.
Understanding the roles of the FDA, study sponsors, contract research organizations, coordinators, and investigators provides the framework of study design and implementation.
Between those two poles lies a realm of environmental and pragmatic considerations that reflect the goals, biases, risk-tolerance, and constraints of study sponsors and organizers.
In contrast, participants from the lower-income, higher-minority communities assessed health studies with reference to their trust (or lack thereof) in study sponsors and public health institutions.
The study sponsors had no role in the design or conduct of the study, in the collection, analysis, or interpretation of the data, or in the writing of the report.
The study sponsors were the University of Birmingham and Birmingham Women's NHS Foundation Trust, and the study was funded by the National Institute of Health Research NIHR Health Technology Assessment Programmeme (06/404/84).
Clinical investigators or study sponsors often face challenges when designing clinical trials on human cells and tissue products with the goal of obtaining premarket approval owing to the unique characteristics of products in this category.
The study sponsors did not influence the study design.
Study sponsors, particularly from industry, may not agree to release raw detailed information.
The study sponsors did not play any role in design or implementation of the study.
