MainEDC™ eClinical Solution for Medical Research
of any Complexity

Faster, clearer, transparent clinical trials
with scalable powerful platform
trusted by 136 Pharma, Biotech and CROs

Get Free Trial



Platform

  • Deploy studies in days: median FPI 9.2 days after start. Ready-to-use tools, templates and best DM/DS practices 
  • Save budget: up to 85% off on a platform (EDC, ERT, eCOA) and up to 75% off on clinical monitoring
  • Best price on the market:
    Fixed, Fair and Open!

IRT / eCOA

  • All types of randomization and dose regimens (our own patent for Dynamic Randomization)
  • Automate the drug supply management – significantly mitigate the human factor risk (noted by 97% of customers)
  • Compliance is up to 99.4% using active eCOA SMS/Push reminders.

e-Training

  • Build your first study during the training with our experienced DM   
  • Increase the knowledge and advancement of Data Management and Data Science professionals (noted by 96,6% of specialists)
  • Back up your team with resources at any step - Data Managers, Data Science, Personal Mentors 

Decentralized patient-centric, hybrid, or traditional clinical trials of all phases


Premium security level,
private cloud hosting

GCP E6 R2, GAĚP 5, 21 CFR Part 11,
GDPR, HIPAA compliant

Prompt and easy eCRF building,
advanced Visual Edit-checks Builder


MainEDC™ ePRO ( Electronic Patient Reported Outcome) for Capture Patient Data

Easy access for investigators via www.yourcompany.investigator.site

Transfer of Competence

Transfer comprises sharing of DM 365's expertise in data management, data science or drug management through our mutual work on a particular project of yours - typically, your first one with MainEDC™. We will offer you the optimal solution for your situation.


Transparency at every step
of working on the project

Best practices, useful techniques and knowledge
sharing

Îngoing support
and analytics

Let's have a conversation about your solution

MainEDC™ platform is compliant with industry standards and international regulations

  • ICH GCP E6(R2)
  • HIPAA
  • GDPR
  • 21 CFR Part 11
  • GAMP 5
  • CDISC
  • MedDRA

Articles

You make great medication.
We help make it affordable by speeding up clinical trials and reducing development costs. 

Let's talk