Are you a sponsor forced to change the CRO on an ongoing project? We will do the data migration without stopping the study.

From time to time, clients task the DM365 team with importing clinical data collected outside of MainEDC: from eSource, Excel spreadsheets, another EDC system that for various reasons the client decided not to use. As a result, we need to get a ready-to-use eCRF in the MainEDC system with automatically uploaded data.

In the end of the 2022 year Creative Pharma Company selected DM365 to be EDC vendor for their projects. We’ve asked Giorgos Tsakonas, Medical Data Manager a couple of questions about the upcoming partnership: What prompted the search for a new EDC vendor?  We were looking for a new, cost-effective, simple but yet powerful EDC provider for our new projects. MainEDC fulfills all of our standards to be the “tool” we choose to use for our trials. What do you expect from working […]

MainEDC™ has been awarded a Summer 2022 Top Performer Award by SourceForge, the world’s largest software and services review and comparison website. This award recognizes exceptional companies and products with a significant amount of recent favorable user reviews that puts them in the top tenth percentile of highly reviewed products on SourceForge. To win the […]

In blinded trials, there are some situations where planned or unplanned unblinding is required. We decided to have a look at unblinding processes and share some thoughts from our experience.

There is no need to say that every EDC business process could suffer from human error. Unfortunately, there is no way to prevent it, but there are ways to improve the process of data corrections.

We are excited to share our accumulated experience in the migration of data and eCRF structure in clinical trials

Save up to 75% of clinical monitoring costs

Data Management 365 is pleased to announce the evolutionary company transfer to Data Science standards.

Data managers all over the world come across this question: how to handle the codes already assigned to eCRF terms when the next MedDRA / WHODrug version becomes available. Here is the answer