Our services
Phases 1-4
Administrating all clinical trial phases
At the American Institute of Research, we conduct phases 1, 2, 3, and 4 of the clinical trial process. We make sure to conduct these clinical trials by maintaining the highest levels of ethical behavior.
Follow-up
Patient follow-up
We care deeply for our patients and their health. After one of our patients' participation in one of our clinical trials is over, we make sure to check up on them. Patient safety is a priority at the American Institute of Research.
Negotiations
Contract & Budget negotiations
At the American Institute of Research, we conduct phases 1, 2, 3, and 4 of the clinical trial process. We make sure to conduct these clinical trials by maintaining the highest levels of ethical behavior.
Data entry
Precise & accurate data entry
The American Institute of Research has a qualified data entry team that makes sure to input patient data with the utmost level of accuracy and precision.
Protocols
Ensuring protocol compliance
Ensuring protocol compliance and conducting the study in the most efficient and effective way possible is always our goal. Adhering to the protocol and conducting ongoing training for amendments if applicable is what we do best.
Archival
Trial-related Documents Archival and Maintenance
We make sure to archive all of our patients documents with the greatest of care, and make sure to maintain them. We will never lose track of one of our patients' documents.
Initiation & Close out
Site initiation & trial close-out operations
We strive to accommodate SIV’s within the sponsors' needed timelines in order to assure patient enrollment into each trial as quickly as possible. Our close out visits are conducted effortlessly between the clinical team, regulatory team and the investigators.
Approval
IRB/IFC Approval
AIR’s regulatory team maintains great relationships with most IRB’s across the nation. This allows us to request expedited reviews in most situations
Submission
Submission for Institutional Review Board or Independent Ethics Committee
AIR’s regulatory team performs ongoing evaluation of the regulatory submissions as well as a 24-hour regulatory turn around if needed to the review board such as initial applications, study status reports, continuing reviews, protocol amendments and any other submission needed per ICH guidelines.
