Research Center Profile:
Greenway Medical Technologies
Cardiology/Vascular Diseases
Dermatology
Devices
Endocrinology
Family Medicine
Gastroenterology
Immunology
Infections and Infectious Diseases
Internal Medicine
Musculoskeletal
Nephrology
Neurology
Nutrition and Weight Loss
Obstetrics/Gynecology (Women’s Health)
Ophthalmology
Orthopedics/Orthopedic Surgery
Otolaryngology (Ear, Nose, Throat)
Pediatrics/Neonatology
Psychiatry/Psychology
Pulmonary/Respiratory Diseases
Rheumatology
Sleep
Urology
Vaccines
Greenway Medical Technologies is an Electronic Health Record (EHR) company that provides its EHR software solution to thousands of practice physicians in ambulatory care settings across the US.
Contact us today to learn more about how using sites with electronic health records is changing the face of research by targeting investigator site selection, reducing manual chart reviews for eligible patients, providing easier access and accountability for monitoring and data capture.
Greenway's PrimeRESEARCH Site Network is comprised of research sites that take advantage of our "EHR Enabled Research" capabilities which include:
- Site database queries that identify which sites have the patient population required by the protocol
- Queries that use the protocol inclusion/exclusion criteria which will instantly identify which patients match protocol eligibility, reducing chart searches and time to enrollment
- Easy access to feasibility data from our database of over 8 million patients
- Mapping data directly from patient's electronic health records into EDC using the CDISC standard known as RFD or Retrieve Form for Data Capture
- Remote monitoring of source documents- monitors can log in to a secure view of site source documents, reducing the time and travel required to view patient records and perform SDV
PrimeRESEARCH Site Network
All PrimeRESEARCH sites use Greenway's EHR, enabling them to receive study opportunities by taking advantage of our "EHR Enabled Research". Study sponsors and CROs contact us about study opportunities, and after running database queries across our site network, we can provide targeted site information for ease of site selection. There is no cost for this service to sponsors or CROs.
PrimeRESEARCH Sites are independent, experienced clinical research sites that conduct phase 2-4, registry, and observational trials. Sites sign their own study contract and are paid directly by the sponsor or CRO. Network study capabilities include most therapeutic specialties except for oncology. We make finding the right site, with the right patient population easy. Sponsors have selected as many as 300 PrimeRESEARCH sites for a single study.
Data Mapping (RFD) from EHRs into EDC
PrimeRESEARCH is the first and only site network to have completed 3 studies using the RFD standard where data was mapped directly from patient electronic health records into the EDC. This eliminates some of the duplicate data entry required to complete EDC CRFs and reduces source document verification (SDV). RFD can be utilized for clinical trials, post marketing data and safety data capture such as MedWatch completion. RFD is an option for data capture that will continue to develop as a technological advancement in conducting clinical trials.
Remote Monitoring for Source Document Verification (SDV)
PrimeRESEARCH is the first and only site network to enable remote monitoring of patient source documents. Monitors are given a secure, restricted view of (enrolled only) patient records. A full audit trail report documents which sections of the patient record were monitored and can also be used to document monitoring visit "trip reports". Remote monitoring increases the ability of monitors to perform SDV more frequently, without the burden of travel. Remote monitoring provides the sponsor/CRO with more-transparency, and investigator site oversight, while significantly reducing the cost of monitoring visits. Remote monitoring is an optional service provided to sponsors and CROs. Monitoring patient medical records is conducted in the same manner, but with a reduction in travel time and expenses.
If you are interested in contacting this center to discuss placing a clinical
trial there, please complete and send the email form below. A representative from
the research center will then follow up with you.
