Seattle, WA (PRWEB) July 22, 2014
Quorum Review IRB, the industry leader in central IRB services, announces a new service for large clinical trials called Quick Step™. The offering went live on July 1, 2014 and is designed to address the research industry’s need for seamless study start-up with a large volume of researcher sites. The service is available for studies planning 50 or more North American investigator sites, as well as related studies with a combined planned North American site count of 80 or more. Qualifying studies may also enroll international sites after the minimum for North America is met.
The Quick Step™ program bundles efficiency features that only an IRB of Quorum’s expertise and size can offer. Quick Step™ includes a study manager that is assigned before IRB submission; five hours of complimentary regulatory consulting from one of Quorum’s six in-house attorneys; facilitated completion of our Central Study Questionnaire (CSQ); identification of potential sites for enrollment; and assisted site outreach. Additionally, for the purpose of site enrollment, Quorum can migrate certain site data from related studies already under Quorum’s oversight, as well as data from other IRB forms for studies being transferred to Quorum.
The first stage in Quick Step™ is the assignment of a Quorum Study Manager (in advance of study submission) to help clients expedite and customize their submission process for review. The Study Manager also helps clients determine how best to use their five hours of complimentary regulatory consulting—perhaps for protocol/consent discussion or
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