Can I use my own consent forms?
Yes. Upload your consent form or use our template to configure various fields recreate your own.
How simple is it to set my study?
Set up is an easy, one-time activity that can be done within 24-72 hours of project initialization
Does 5thPort support integration to other systems?
Yes. 5thPort can integrate with any clinical trial management system and EMR with ease.
Does 5thPort provide the multimedia materials?
Yes. The system is designed to support videos, quizzes and custom documents that you may need for your study. We have partnered with Healthwise, the healthcare industry’s leading developer of content and patient education solutions, with access to a library of medical videos that can be leveraged.
My trial has multiple sites with different jurisdictions. Can 5thPort support multiple IRB’s for a single study?
Yes. 5thPort can easily support multi-site trials. The system can be configured to allow the PI or study manager to set up the trial and also determine the necessary staff across different sites who would be eligible to participate in the trial. 5thPort is designed to be used AFTER an IRB approval is obtained by the CRO. The system can be set up to allow each trial site to have its own settings and branding. Additionally, different IRB requirements can be supported for the same study.