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Data Capture, Simplified.
mEDC is a web based electronic data capture system that offers faster study setup, flexible
configuration, detailed reporting, improved query management, all leading to enhanced
user experience.
Value Differentiation
Other EDC mEDC
Price Ease of Use CRF Design
Complexity
Compliance 24x7 support Deployment
time
Integration with
other systems
Security Training
requirements
Domain
expertise
Technology
expertise
Integrated Data
Management
Service
LowHigh
Key Features
Core CDMS functionality: Study design, Set-up, Edit checks,
Discrepancy management, Database lock and Archival
Single/Multi-site management
Detailed dashboard & reports
Built-in auto medical coding
Fully compliant with FDA 21 CFR Part 11 and GAMP 5
Supports univariate and multivariate edit checks
Intuitive role-based views and displays
Data exports to SAS, CDISC, CSV, XML and Excel
formats
Complete audit trail
24/7 Tech Support
Key Benefits
Create eCRF forms with ease without programming: An unique interface for
stakeholders to design and create complex CRF forms easily.
Highly configurable and adaptable: To accommodate the best practices in
clinical trials, and can be easily customized for any specific study phase or
therapeutic area.
Run adaptive trials and implement protocol amendments quickly: Sponsors
can now deploy all mid-study amendments without compromising study
database integrity. mEDC manages multiple CRF editions and seamlessly
migrate existing data into new forms and visit structures.
Rich, intuitive user interface: User friendly, easy navigation and rich graphical
interface with robust features ensures high acceptance by the stakeholders.
Increased data accuracy and reduced cleaning time: With sophisticated edit
check programming and auto medical coding feature.
Seamless integration with third-party systems: Easily shared with other
clinical systems like IWRS, IVRS, CTMS, ePRO and drug safety systems.
Lower total cost of ownership: Easy to install and set-up, and requires less
programming/technical knowledge. With flexible deployment options and
support services, mEDC is best ROI which truly reduces the client’s total cost of
ownership.
Simplified eCRF creation
Multi-lingual
Improved data quality
Highly configurable
Quick amendments
Better decision making
Increased data accuracy
Reduced cleaning time
On-demand ad-hoc reports
Seamless integration with
third-party systems
For a product demo, please reach us at:
info@DDIsmart.com or www.DDIsmart.com USA  EUROPE  ASIA
DDi (Drug Development informatics) specializes in providing clinical
informatics and IT solutions to Life Sciences industry. As a global drug
development partner serving the Life Science organizations since
more than a decade, DDi leverages its rich functional domain expertise
and technology competency to design and build innovative solutions
for Pharmaceutical, Biotech, Medical Devices and Research institutes.

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mEDC_Single

  • 2. mEDC is a web based electronic data capture system that offers faster study setup, flexible configuration, detailed reporting, improved query management, all leading to enhanced user experience. Value Differentiation Other EDC mEDC Price Ease of Use CRF Design Complexity Compliance 24x7 support Deployment time Integration with other systems Security Training requirements Domain expertise Technology expertise Integrated Data Management Service LowHigh Key Features Core CDMS functionality: Study design, Set-up, Edit checks, Discrepancy management, Database lock and Archival Single/Multi-site management Detailed dashboard & reports Built-in auto medical coding Fully compliant with FDA 21 CFR Part 11 and GAMP 5 Supports univariate and multivariate edit checks Intuitive role-based views and displays Data exports to SAS, CDISC, CSV, XML and Excel formats Complete audit trail 24/7 Tech Support
  • 3. Key Benefits Create eCRF forms with ease without programming: An unique interface for stakeholders to design and create complex CRF forms easily. Highly configurable and adaptable: To accommodate the best practices in clinical trials, and can be easily customized for any specific study phase or therapeutic area. Run adaptive trials and implement protocol amendments quickly: Sponsors can now deploy all mid-study amendments without compromising study database integrity. mEDC manages multiple CRF editions and seamlessly migrate existing data into new forms and visit structures. Rich, intuitive user interface: User friendly, easy navigation and rich graphical interface with robust features ensures high acceptance by the stakeholders. Increased data accuracy and reduced cleaning time: With sophisticated edit check programming and auto medical coding feature. Seamless integration with third-party systems: Easily shared with other clinical systems like IWRS, IVRS, CTMS, ePRO and drug safety systems. Lower total cost of ownership: Easy to install and set-up, and requires less programming/technical knowledge. With flexible deployment options and support services, mEDC is best ROI which truly reduces the client’s total cost of ownership. Simplified eCRF creation Multi-lingual Improved data quality Highly configurable Quick amendments Better decision making Increased data accuracy Reduced cleaning time On-demand ad-hoc reports Seamless integration with third-party systems
  • 4. For a product demo, please reach us at: info@DDIsmart.com or www.DDIsmart.com USA  EUROPE  ASIA DDi (Drug Development informatics) specializes in providing clinical informatics and IT solutions to Life Sciences industry. As a global drug development partner serving the Life Science organizations since more than a decade, DDi leverages its rich functional domain expertise and technology competency to design and build innovative solutions for Pharmaceutical, Biotech, Medical Devices and Research institutes.