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Our mission is to deliver best value to the benefit of patients,clients,employees and government through
innovation,trust,speed,quality,global orientation,sound business management and dedication to excellent service. |
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MENE EDC provides the life science industry with a unified solution for clinical data collection , built on one unifying database layer which includes, but is not limited to eCRF, eDiary , patient compliance , trial- and supply management systems from the ground up: better, smarter, faster – and still at affordable cost. Today we’re ready. Tomorrow we could be talking.
Experienced, high caliber, and well trained professionals.
- Decades of acquired expertise
- Worldwide offices in Europe, Asia and North America
- Global 24/7 multilingual support
- Secure and redundant Application Service Provider (ASP)
hosted solution
- Comprehensive training including eLearning, remote sessions
and face-to-face solutions
- Enterprise-wide Quality Management System
Regulatory Compliance
All MENE EDC products & services are compliant with all current
regulatory and privacy directives
Experienced Support by Domain Experts
Our personnel have extensive technical and clinical experience. They
understand how to translate your clinical data requirements into a well
designed eCRF and dataset deliveries because they understand your
language and your needs from a clinical perspective. Our project
managers and technical design consultants have an average of over six
years of eClinical experience.
We believe in building long-term partnerships through commitment to
quality service by providing you the best, most experienced personnel
available, strong management support, honest communications and
transparency in all of our dealings.
unithink is committed to supplying products and services that are secured
by our enterprise-wide Quality Management System (QMS) with the key
focus on continual improvement through adoption of best practices
across all processes.
Accelerated Trial Development
We understand that rapid deployment is important to our clients. Our
design tool supports rapid development because it does not require
extensive programming skills, rather your trial is created using drag and
drop configurability.
Our web-based design tool allows multiple designers to configure a trial
simultaneously. We will employ adequate resources to meet your
timelines. We deploy design and quality control testing resources
throughout our EDC specific worldwide offices in Belgium, India, USA and Germany
which allows for continuous development 24-hours a day when needed.
Adaptive to Fit Each Trial’s Specific Needs
Access to particular sites and data can be controlled down to a single
field based on role definition. MENE EDC allows for the same users to
have different roles and restrictions in each trial. As you add additional
trials in the future, access to all trials will remain through the single log
in. Workflow and role responsibilities can be configured to match your
processes and adapt to evolving research processes instead of having
to comply with rigid system requirements. Configurable page layouts
allow more data to be shown in a familiar format with less scrolling,
reducing errors and allowing for faster data entry and cleaning.
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