Diabetes
December 28, 2018
Yes. Our office has 1 dedicated monitor rooms, as well as a private office, that can be used for monitoring purposes. All monitor space is equipped with separate high-speed internet access, printers and common office supplies.
Yes. Our office is equipped with state of the art print/copy/scan/fax machines. It is located next to the monitoring rooms in a convenient location
8 AM to 6 PM; Monday – Friday and Open during weekends if required by the protocol.
Yes. Our CLIA-waived certified lab is fully equipped with a centrifuge, -20 degree, phlebotomy station, 24-hour temperature monitoring, ECG, HbA1c, Microscope, storage space for all study specific lab equipment and a computer with printer/fax/scan.
We use CTMS for our Clinical Trial Management System. Currently, we have over 4000 active research patients and growing. We have access to our investigators patient database around 15000 active patient list.
Yes, we use EPIC EMR.
We appreciate scheduling monitor visits with 2 weeks notice, but we are able to accommodate our monitors in case of emergency or extraordinary circumstances.
Yes, Most of the studies we have conducted over the past year have used EDC. Our staff is experienced in InForm Phase Forward, Oracle, Medidata Rave, Open Clinica and Axiom. Our site also has a dedicated data / QA specialist.
IVRS experience includes ICON, ClinPhone, UBC and Medpace.
Yes. Most of our studies are require electronic diaries. Our staff is well trained to teach and train patients in e-Diaries and iPhone / Android Mobile Apps
Agile CRT believes in a multi-strategic approach to patient recruitment. We have been very successful with local advertising. In addition, we recruit participants from our database and participate in local community outreach events such as: health fairs; health clubs; physician referrals;
Our online recruitment on our website; social networking; blast emails; adwords; and word of mouth referrals. We have our own social media advertisement platform tailor to our patient recruitment.
We believe retention begins at the very beginning of the process with subjects having a full understanding of the clinical trial requirements. An open door communication between subject, coordinator and investigator paves the way for good retention.