ABOUT MEDNET
Mednet is a leading healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for over 21 years to deliver the technology innovation, experience and reliability they need for success.
Mednet’s comprehensive, EDC-centric eClinical platform, iMednet, optimizes clinical studies of all types and sizes – accelerating research with exceptional flexibility, ease-of-use, robust functionality, affordability, and stellar support. iMednet is feature-rich and uniquely designed to help sponsors and CROs get studies up and running quickly and to see them through with a full suite of native capabilities, including: randomization, trial supply management, adjudication, ePRO, payments, and DICOM Imaging. All backed by a highly tenured and experienced support team, ensuring quality, compliance and easy onboarding of the entire research team and clinical trials sites.
iMednet provides scalable pricing and a menu of modules where you can implement only what your study requires, while also enabling integrations as needed. This type of solution can support the requirements of both early and later phase studies, while also providing pricing flexibility and transparency, so you only pay for the modules you need. It can also smooth the transition to later stage trials while masking the complexities of powerful functionality behind simple user interfaces.
Mednet makes it easy to export or import clinical trial data. Whether through its Data Import Manager or API, iMednet is designed to efficiently share data with other systems and effectively meet the evolving demands of today’s study designs and requirements. iMednet API allows clinical research teams to easily integrate with a wide range of clinical research technologies, including CTMS, eCOA, eTMF, eConsent and more.
FEATURED ARTICLES
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Coordinating and centralizing eClinical platform functionality is essential to enabling agility and flexibility in the modern clinical trial landscape.
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Developing life-saving heart health treatments requires an understanding of the unique requirements of cardiovascular studies, along with flexible eClinical and electronic data capture solutions.
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With adjudication, learn how teams can enhance the quality and integrity of their research, paving the way for impactful and reliable outcomes in clinical research.
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Clinical studies are pivotal in understanding cancer—its prevention, detection, treatment, and cures. Learn to enhance efficiency in complex oncology studies with the right technology and guidance.
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Understand how the Clinical Data Acquisition Standards Harmonization works to support the integration of research into the clinical workflow.
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Growing more widespread in clinical research, adaptive trial designs allow for prospectively planned modifications but tend to require versatile technology to support these studies' complex and ever-changing nature.
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Gain insight from the challenges, recent progress, and clinical trial needs in the rare disease sector and how technologies and supporting procedures will determine how quickly and effectively new medications can get to market.
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Learn how a seamless payments solution can help clinical trial sponsors improve site satisfaction with automated payments, real-time status updates, and quick, easy resolutions to payment issues.
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When choosing a technology partner, CROs should consider the partner's experience in the clinical research industry, ability to meet the CRO's specific needs, commitment to quality, and more.
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Efficiencies in ophthalmology studies can be improved by automating tasks, streamlining workflows, and providing real-time data insights. Learn how technology can help researchers to accelerate the pace of research, improve the quality of data, and reduce costs.
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Choosing a clinical technology partner is a big decision. Ask these questions when determining if a potential candidate is the right choice to build a study (or studies) on their own.
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Take notes from this multi-dimensional customer success model to enhance your readiness to address a diverse array of customer requirements and needs effectively.
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Technology is playing an increasingly important role in clinical trials, helping to improve efficiency, compliance, and data quality. Learn why it’s critical that clinical study technologies are easy to use across sites and fit into the team’s workflows.
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Choosing the right eClinical solution can be difficult. Consider a platform’s various capabilities when deciding on a solution that performs and supports clinical trials at every study phase.
CONTACT INFORMATION
Mednet
601 Carlson Parkway, Suite 250
Minnetonka, MN 55305
UNITED STATES
Phone: (866) 258-2735
SOLUTIONS
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Simplify And Elevate The Participant Consent Process
Designed to accommodate the diverse requirements of traditional, hybrid, and decentralized clinical trials, see how this eConsent solution is able to guarantee a user-friendly experience across all devices.
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iMednet Enhances Visibility & Streamlines Adjudication
Learn about iMednet Adjudication’s valuable assistance in addressing escalating regulatory expectations for independent adjudication, intricate study designs, and diverse endpoints.
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Take Full Control Of Site Payments With iMednet Payments
iMednet Payments offers a swift automation solution, enabling study administrators to effortlessly manage site-specific study budgets, review and authorize eligible payments, and access a comprehensive transaction history, all efficiently and error-free.
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iMednet Optimizes Randomization & Trial Supply Management
Improve efficiency and study start-up speed, and maximize results with seamless randomization and trial supply organization modules.
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Accelerate Study Start-Up With Flexible EDC Technology
Enable researchers to quickly and accurately collect patient data in real-time, and eliminate the need for paper-based data collection methods, saving time and reducing the risk of errors.
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Introducing iMednet
Optimize clinical trials with iMednet, a comprehensive, clinical data management system, centered around a robust EDC with key native modules.