Chesapeake IRB

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Chesapeake IRB has built a reputation for excellence based on quality work, efficient processes, and excellent customer service. Chesapeake IRB’s schedule of 5 weekly meetings, daily expedited review capability, 4 day turnaround for protocols and 24-hour turnaround for Principal Investigators (PIs) has helped our clients become more competitive for industry sponsored studies; including Phase I research. While the majority of our studies are biomedical or device related, we have a broad range of social/behavioral studies that are often government or foundation funded. We work with you as a risk mitigation.

chesapeake irb clinical research ethics phase i-iv clinical studies cirbi institutional review board services independent irb services aahrpp jeffrey wendell patient advocate investigational review board patient safety compliance clinical services data protection clinical trial data management fda clinical site clinical study irb ellen kelso informed consent protection of research subjects social media ruth boulter confidentiality participant compensation ethics irb services declaration of helsinki ethics clinical research ethics united states and canada phase 0-iv clinical study virtual irb management platform felix gyi pharm d independent irb

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Chesapeake IRB

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Chesapeake IRB

Chesapeake IRB: Risk and Harm in Research

Chesapeake IRB: The evolution of ethics in clinical research

Chesapeake IRB & Social Media

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Chesapeake IRB & Social Media