Learn how centralized data can help institutions efficiently and accurately report their research performance and discover the tools to help.
Join over 200 clinical research professionals for informative sessions, valuable networking opportunities, tips for getting the most from your Forte technology.
As natural and man-made disasters have become more prevalent in the healthcare industry, it’s important for research organizations to ensure they have well-defined business continuity and disaster recovery plans.
Whether using paper, shared drive or vendor-provided systems to manage regulatory documents, research organizations need to ensure their data is safe in the event of a natural disaster.
Clinical research technology can provide a foundation to streamline operations and help you reach your full research potential. Learn how these systems give you visibility into your research, boost compliance, manage your data and much more.
Integrating your clinical trial management system and general ledger system can help provide your institution with a complete picture of the financial health of your protocols.
Learn how an eRegulatory-CTMS integration can improve workflows and bring additional benefits to your institutional research operations.
There’s a better alternative to manually building protocol calendars in your CTMS. Learn how your research site can work smarter, not harder.
Don’t overlook these key factors when making your build vs. buy decision for a research evaluation and reporting system.
Choosing the right CTMS can enhance your billing compliance and minimize risk.