Frequently Asked Questions

We specialize in negotiating Clinical Trial Agreements (CTAs) for clinical research sites. Our expertise ensures your site secures fair and favorable terms that align with your financial goals and operational needs.

Our contract and budget negotiation process typically takes about two weeks to complete. However, timelines may vary depending on sponsor and CRO responsiveness. We proactively manage communications to keep the process moving as efficiently as possible.

At Reatrix, LLC, we understand that every research site is unique, which is why our services are tailored to your specific needs. We offer customizable pricing packages designed to fit your site’s budget and operational goals. We also believe in transparent pricing—check out our pricing brochure to get an idea of our rates. Keep in mind, we're always willing to work with you to create an affordable solution that meets your needs.

We offer customizable financial reports designed to provide clear insights into your site's revenue. Reports can be delivered yearly, monthly, weekly, or even daily, based on your preference. Our detailed breakdowns can organize data by sponsor, therapeutic area, or other criteria, making your financial information easier to track, understand, and present.

Our full site support services are designed to lighten your team's workload, allowing you to focus on study procedures and patient care. Whether you need minimal assistance or full-scale support, we adapt to your needs. Our services include:

• Study Startup – Budget development, contract execution, and site activation
• Regulatory Maintenance – IRB submissions, document updates, and compliance tracking
• Data Entry and Management – Ensuring accurate and timely data submission
• Ongoing Support – Assistance