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EasyMedStat

Data collection, statistical analysis, and publication-ready reporting for clinical research studies.

Solution by EasyMedStat
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Overview

EasyMedStat is a clinical research platform designed to support the full study workflow, from data collection through statistical analysis to publication-ready outputs. It is used by academic institutions, medical device companies, and medtech and biotech organisations conducting prospective studies, retrospective studies, registries, and post-market clinical follow-up (PMCF) studies.

The platform centralises data management, patient inclusion tracking, data quality assurance, and regulatory compliance in a single environment. Over 300 peer-reviewed journal articles have cited EasyMedStat, and more than two million patients have been analysed using the tool.

Electronic Case Report Form (e-CRF)

  • Provides a customisable e-CRF that can be configured and deployed in minutes.
  • Supports data import to migrate existing databases into the platform.
  • Designed to be configurable by non-technical users, including clinicians.

Statistical Analysis

  • Covers descriptive statistics, univariate analysis, and multivariate analysis.
  • Automatically selects the appropriate statistical test based on the data distribution.
  • Guides users through the analysis process without requiring specialist statistical knowledge.

Publication and Reporting Outputs

  • Automatically generates formatted statistics suitable for inclusion in articles and reports.
  • Produces professional charts ready for use in publications.

Study Types and Target Users

  • Supports academic institutions running multicentric, prospective, and retrospective studies.
  • Supports medical device companies conducting PMCF studies, registries, prospective studies, and retrospective studies.
  • Supports medtech and biotech organisations with the same range of study types, with an emphasis on autonomous delivery.

Platform Characteristics

  • Operates within a secured environment.
  • Designed to meet regulatory compliance requirements.
  • Reported average time to start a study is four weeks.

EasyMedStat is available in English and French and can be accessed via account registration or a booked demo. The platform is positioned for both individual researchers and larger clinical research departments within hospitals and private healthcare groups.

Meta

Domain
Clinical Trial Management
Subdomain
Electronic Data Capture (EDC)
Software type(s)
Analytical Platform
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
Academic / ResearchBiotechMedical DevicesPharma
Development stage(s)
ClinicalPost-Market & RWE
Target user(s)
Research ScientistQA / Regulatory AffairsClinical / Diagnostic Professional
Compliance standard(s)
GxP