Participating in a clinical study at BioResearch Partner is a guided, transparent process designed around patient safety, comfort, and communication. From your first contact through study completion, our teams are here to support you every step of the way.
Once you express interest in a study, our team will reach out to learn more about you and determine whether you may qualify. This step may include a brief phone call or questionnaire to review general health information and study criteria.
There is no obligation to participate during this stage.
Before any study-related procedures take place, you will review and sign an informed consent document. This document explains:
Our staff will take time to answer all questions so you can make an informed decision.
If you qualify and choose to participate, you will attend scheduled study visits at one of our research sites. During visits, you may receive:
All visits are conducted by experienced medical professionals in a controlled clinical environment.
Throughout the study, our coordinators remain available to support you. You will receive reminders for appointments, clear instructions for each visit, and continued communication about what to expect next.
Your safety and well-being are monitored closely throughout participation.
After completing the study, our team will guide you through any required follow-up visits or final evaluations. Participation may help advance medical research and improve future treatment options for others.
You may also be informed about other studies you could qualify for in the future.
Participation in clinical research is always voluntary. You may choose to withdraw from a study at any time. All studies conducted at BioResearch Partner follow strict safety, ethical, and regulatory standards.
Explore current studies or speak with our team to learn more about participating in clinical research at BioResearch Partner.