Investigators

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Opulink emphasizes timely management of the front-end aspects of clinical trial studies while also following through on all day-to-day developments until study completion and closure. Specifically, the staff at Opulink is deployed to expedite completion of regulatory documents and IRB approvals, facilitate study initiation, speedily recruit and enroll patients and ensure safe management and transfer of any confidential data or records to our clients.

We maintain intimate contact with our investigative sites, requiring regular documentation on the status of clinical trials including the assurance that the highest standard of ethics and scientific integrity are adhered to continuously. Patient recruitment is not a single activity but rather a host of responsibilities.

Additionally, as part of our comprehensive abilities to forecast, we manage patient recruitment, by providing our sites with site-support services such as “CureBridgesm” and other forms of assistance in assuring timely completion of study status reports, case report forms and organization of data.

CureBridgeSM is a database which contains people who have voluntarily expressed interest in being in clinical trials…not just a list of names, but actual data entered by people who want to participate. These potential participants have learned of the database from Opulink’s various programs which inform and educate people at a “grass-roots” level about the benefits of participating in clinical studies. People in the database cover the continental US, Alaska, and Hawaii.

We are particularly adept at bring together other resources and components of the clinical trial investigative practice to accomplish the objectives of our clients.

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