Data Management 365

DM365 present an automatic project publishers built into the MainEDC™, which allows users to control the process of eCRF creation and transfer them

Publisher: a new component of the MainEDC™ system

5 Ways to Implement ePRO (electronic Patient Reported Outcome) in Your Clinical Trials

5 Ways to Implement ePRO (electronic Patient Reported Outcome) in Your Clinical Trials ePRO (or eCOA – Electronic Clinical Outcome Assessment) is a software that allows patients to share information with investigators via their own electronic devices using a mobile or web application instead of paper forms.

Data migration in clinical trials

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

Data migration in clinical trials 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

Save up to 75% of clinical monitoring costs Save up to 75% of clinical monitoring costs

We are pleased to announce the evolutionary company transfer to Data Science standards!

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

Quick summary of a few scenarios that require unblinding along with some tips on how to better configure unblinding procedures.

Subject Unblinding in Clinical Trials. MainEDC Story of Experience 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.

The coding process could be very complicated, and we aim to make it as simple for you as possible!

MedDRA and WHODrug up-versioning: MainEDC™ helps with the coding in long-lasting studies 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

Data change requests processing is a standard workflow where EDC & IWRS systems are in use. We made it really user-friendly and still compliant with applicable regulations (21 CFR p11, GCP).

Cost reduction of human error in EDC business processes with automated electronic Data Change Requests 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.

The most cited medical journal in the world published an article featuring as the provider for one of the largest clinical trials ever conducted!

Data Management 365 in The Lancet journal The most cited medical journal in the world, The Lancet, published an article featuring DM 365 as the provider of the electronic platform for one of the largest clinical trials ever conducted.

Eight months of development and testing followed by six highly loaded projects, and voilà! Today, we're excited to introduce the brand new advanced and fully integrated MainEDC™ ePRO platform.

Follow the link to learn more.

Data Management 365 MainEDC™ ePRO Get in touch with us for 15% discount for MainEDC™

MainEDC passed the toughest test – supported three Phase III clinical trials with 40 000, 25 000 and 12 500 subjects loaded – some of the largest trials in history so far.

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