Meeting in the Midwest: Welcome to the 2017 Fall Onsemble Conference
Attendees gain actionable insights during the first two days of Forte’s 2017 Fall Onsemble Conference in Madison, WI.
Standardization and the Importance of Medical Coding Dictionaries in Clinical Trials
Medical coding dictionaries standardizes data interpretation, which increases data quality and minimizes risk.
The Professional Research Subject: Fact or Fiction?
Can participating in clinical trials be a full time job? A look at the impact money has on enrollment decisions.
How to Start Effort Tracking at Your Clinical Research Site
Use these six simple steps to implement effort tracking at your clinical research site.
Navigating the Gray Areas of Delegation of Authority: Informed Consent
Knowing when to delegate a task to qualified research staff isn’t always straightforward. Learn why navigating the gray areas of delegation of authority can be particularly problematic.
Payments to Research Subjects: What is Taxable Income?
When are subjects required to report payments received from clinical trial participation to the IRS, and what is the research site’s role in 1099 reporting?
[Q&A] How to Navigate the Impacts of Recent Updates to the CCSG Guidelines
Webinar presenter, Regina Schwind, answers attendee questions following her presentation on recent updates to the CCSG guidelines.
Tips for Improving Your Delegation of Authority Processes
How to standardize and streamline the delegation of authority process for more efficient and compliant task management.
Creating a Short List: The Next Phase of Selecting the Right Research Technology
If your organization is beginning the evaluation process for technology vendors and starting the purchasing process, use these steps to help you be confident the system you choose is the right one.