Educational Clinical Research Resources
Meeting in the Midwest: Welcome to the 2017 Fall Onsemble Conference
Standardization and the Importance of Medical Coding Dictionaries in Clinical Trials
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The Professional Research Subject: Fact or Fiction?
How to Start Effort Tracking at Your Clinical Research Site
Introducing the New Forte
Navigating the Gray Areas of Delegation of Authority: Informed Consent
Payments to Research Subjects: What is Taxable Income?
[Q&A] How to Navigate the Impacts of Recent Updates to the CCSG Guidelines
Informed consent is one of the pillars of ethical clinical research. However, it's not always a straightforward process.
Obtaining consent from potential clinical trial participants requires significant consideration to determine the most ethical way to communicate protocol information, and ensure the individuals understand the consent document language. This series explores methods for standardizing the informed consent process and making consent documents clearer to the general population.