Integrity
Clinical Research is truly a Site Management Organization. We
actually manage the Sites, unlike some who only obtain studies and
do regulatory work.
Listed
below is just a sample of our value added services to you the Sponsor,
CRO, or Site.
We market the
research sites nationwide and obtain contracts.
We complete all
Budget
Negotiations and Regulatory Documents at a Central Location with a 3-5
day turn around time.
We prefer to use a
Central IRB.
We have a Training
Program from Columbia University which is presented along with our
own Customized Training and Workbook Module annually at our sites.
Our CRAs go with
your CRAs to site for initial site visit as well as site
initiation.
We then train the
onsite staff to your protocol specifics and actually assist hands on
with the initial patients being enrolled at each site.
Our CCRAs perform internal QA audits at each site.
Our CCRAs can be available to attend monitoring visit if needed to assure site performance and quality.
Our CCRAs are available to assist with follow-up and query resolution when indicated.
We have the same
uniform SOPs for all our sites.
We
tailor our Services to your needs. Just ask our satisfied Sites,
Sponsors and CROs.
We
tailor our Services to your needs. Just ask our satisfied Sites,
Sponsors and CROs.
