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As we reflect on the past year and all of the platform enhancements our team has achieved, we are energized and ready for today’s clinical research challenges. Take a few moments to learn why you should take a first look – or a fresh look – at iMednet in 2024!

Exceptional Experience and Support – Mednet delivers the most experienced and responsive customer service and quality assurance support in the industry. Relationships, proficiency, and trust are core to our culture and critical to success, no matter how intuitive the platform.

  • Average support tenure with Mednet is over 13 years.
  • Compliance team average tenure is over 16 years.
  • Average customer service grade is over 4.8 (on a 5-point scale)

Seamless Access to Full Suite of Tools – Save time with single sign on access to iMednet’s full suite of native modules including EDC, Randomization, Trial Supply Management, ePRO, Adjudication, Payments, Imaging, and eConsent. Everything you need, at your fingertips.

Ease of Use for End Users – Research coordinators, investigators, monitors, and data managers applaud iMednet’s intuitive tools like user based “to-do” lists and patient record grids with highly intuitive action-oriented record statuses, which maximize efficiency and compliance while minimizing time and effort through the duration of the study.

Ease of Use for Study Builders – Simplify complex builds with tools like drag and drop editor, study replication, reusable forms, edit checks, highly configurable CRFs and CDASH compliant CRF templates. Intelligent build tools enable teams to use wizards and other business logic to quickly design and build a study.

Cost-Effective, Competitive Pricing – iMednet’s feature-rich, robust eClinical solution has been thoughtfully designed with native modules to deliver all the functionality of other major players – at a fraction of the cost – and includes unlimited users and sites.

Highly Flexible and Configurable – iMednet allows clinical research teams to swiftly adapt to a variety of study designs, complex protocols, and to mid-study changes with ease. Flexibility ensures an optimal end-to-end solution for all study types and phases.

Unrivaled Quality and Compliance – With an average tenure of over 16 years with Mednet, our quality and compliance team brings unparalleled expertise to the table. Their invaluable experience shines through in their track record of completing hundreds of client audits across all sectors of the industry.

Adaptable Integration – Whether through its API or Data Import Manager, iMednet is designed to efficiently share data with other platforms as needed. Easily integrate with the full eClinical ecosystem, data lakes, wearables, patient recruitment, analytics and more.

Speedy Deployment – Our customers have the option to build the study themselves with whatever level of support is needed from our team, or we can swiftly build for you. By partnering with our specialized team, studies can be up and running in a few weeks versus months.

Reliable and Stable Partnership – Mednet has been in business for over 23 years and is committed to listening, continual improvement, and ensuring long-term customer success. Whether working with a start-up biotech or medical device company all the way through the largest CRO’s – Mednet is a proven, dedicated partner you can rely on.

Contact us to discuss your upcoming clinical trial needs or to request a customized demo of iMednet.