Determining feasibility of a study with instant access to data while saving time, resources, and costs.
“We’ve saved so much time in not having to request approval and that alone has made things very easy for us.”
— DR. NIR HORESH, SHEBA MEDICAL CENTER
Q: HOW DID YOU HEAR ABOUT MDCLONE?
I first heard about the MDClone platform in a presentation when the system was introduced to our medical center. I was impressed with the potential of this tool to help clinicians gather, cross-reference different aspects, and evaluate the data instantly.
Q: HOW LONG HAVE YOU BEEN USING MDCLONE?
I have been using MDClone for more than two years, with growing interest among my colleagues as time progresses.
Q: WHAT HAS MDCLONE ENABLED YOU TO DO?
I’ve been using the MDClone platform in our hospital for a few years now. It has made things very easy to rule out or rule in projects we think there might be some interest in. It enables us to see the size of the cohorts and the size of the sample size of patients in the subjects.
Q: BEFORE MDCLONE HOW DID YOU ACCESS YOUR HEALTHCARE DATA?
Before using MDClone, if I wanted to check whether a study is feasible or not, I had to write an IRB and submit for approval. Usually, it takes a couple of months before we get approval and only after that, will we be able to have access to the data from the hospital medical record. And sometimes, we don’t find anything that suits us as far as the sample size.