Chesapeake IRB has built a reputation for excellence based on quality work, efficient processes, and excellent customer service.
Chesapeake IRB鈥檚 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.
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chesapeake irbclinical research ethicsjeffrey wendellaahrppphase i-iv clinical studiesindependent irb servicesinstitutional review board servicescirbiparticipant compensationethicsirb servicesdeclaration of helsinkiethics clinical research ethicsunited states and canadaphase 0-iv clinical studyvirtual irb management platformfelix gyi pharm dindependent irbpatient advocateinvestigational review boardpatient safetycomplianceclinical servicesdata protectionclinical trialdata managementfdaclinical siteclinical studyirbellen kelsoinformed consentprotection of research subjectssocial mediaruth boulterconfidentiality
We鈥檝e updated our privacy policy so that we are compliant with changing global privacy regulations and to provide you with insight into the limited ways in which we use your data.
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