26 April 2021 News
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
26 April 2021 News
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.
03 February 2021 News
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.
21 December 2020 News
MainEDC™ supports Risk Based Monitoring processes in clinical trials
30 November 2020 News
Decentralized clinical trials, registries, marketing and feasibility projects with the new MainEDC™ ePRO – enjoy two interfaces (phone app and mobile-friendly webpage) working simultaneously with the integrated EDC / IWRS and Drug Supply system!
07 September 2020 News
Data Management 365 journey of implementing LOINC in MainEDC™
08 July 2020 News
A special message from Data Management 365 Operations Director Anna Polikarova in response to COVID-19 – 2020 Hindsight: Had I known about the pandemic beforehand, what would have I done back at the beginning of the year 2020?
11 June 2020 News
28 May 2020 News
04 May 2020 News
Together we just broke the record for the quickest launch of a clinical trial. And now we can share the news!
20 March 2020 News
Data Management 365 urgently releases MainEDC™ COVID-19 Pack, a validated solution that supports clinical research in a pandemic environment.
Emergency changes due to possible deviations from original protocol
Isolation of clinical sites
Work from home
Process continuity support
Accelerated start of COVID-19 projects
For all our current customers, MainEDC™ COVID-19 Pack extension is free!
21 February 2020 News
25 December 2019 News
13 December 2019 News
02 December 2019 News
18 November 2019 News
SDTM (Study Data Tabulation Model) is a standard for Study Data Submission developed by non-commercial industry stakeholders CDISC (Clinical Data Interchange Standards Consortium) . In other words, this is a way how data should be submitted to regulatory agencies.
11 November 2019 News
Our CEO Timur Galimov visited IX Annual International Partnering-Forum "LIFE SCIENCES INVEST. PARTNERING RUSSIA" on November 7-8, 2019.
02 October 2019 News
30 September 2019 News
24 September 2019 Articles
Having fully digital SAE reporting, MainEDC™ lets shorten terms for the safety data submission and decrease the amount of mistakes.