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Leader in soluzioni software per scienziati

iMEDNET - LA PIATTAFORMA COMPLETA PER LA GESTIONE DEI TRIAL CLINICI DALLA A ALLA Z

Sono quasi 20 anni ormai che le organizzazioni farmaceutiche, di dispositivi medici, di biotecnologia e di ricerca a contratto (CRO) di tutto il mondo si fidano di Mednet per ottenere l'innovazione tecnologica, l'esperienza e l'affidabilità di cui hanno bisogno per avere successo.

  • 5
  • buone motivazioni per utilizzare questo prodotto

  1. Implementazione e utilizzo facili e veloci: soluzione innovativa basata sul cloud
  2. Soddisfa dei requisiti normativi sulla protezione dei dati
  3. Adatto a tutti i tipi di ricerca e a tutti i tipi di strutture
  4. Consente la gestione completa degli studi clinici
  5. Consente la visualizzazione dei dati in tempo reale

WHY CHOOSE iMEDNET?

Use iMednet to:

  1. Save time and optimize costs

  2. Facilitate the follow-up and management of your clinical research projects

  3. Focus more on patients

Optimize your clinical trials by simplifying their construction, streamlining data collection and easily adapting them to changing demands

 


Funzioni

iMednet is a complete clinical trial management platform. It is cloud-based and integrates many tools such as data capture, data management and trial management. All you need is located in this platform., iMednet’s native modules are built from the ground up and work together harmoniously without adding cost operation.

DATA CAPTURE

Thanks to the data capture modules in iMednet, you can carry out your studies more easily. The EDC module at the heart of Mednet's unified platform offers complete flexibility and seamless integration with other iMednet modules. Also additional tools such as the ePRO module allow you to collect data directly from patients.

DATA CAPTURE: EDC

You have easy access to everything

iMednet EDC is the cornerstone of all-in-one platform that provides you with the flexibility to build studies very quickly. It easily adapts to complex protocols and changes during the study.

Your study builds are simplified

A highly configurable platform enables complete flexibility, while intuitive tools allow for powerful functionality to implement unique and complex study designs without custom programming.

Ensure the effectiveness of the test execution

iMednet platform allow the entire research team to accelerate clinical trial processes while connecting. Managers have access to capture, cleaning and management of study data throughout the trial. The presence of intuitive dashboards with task lists makes it easy to track and prioritize tasks for key roles.

View in real time the progress of your projects

You can found additional features that help to speed up site start-up activities. Thus, you can access to your data in real time. In addition comprehensive reporting tools allow you to quickly generate the required reports.

 

DATA CAPTURE: EPRO

Ensure compliance and increase patient engagement

The ePRO module of the iMednet platform is accessible anywhere and anytime. This makes it easier to enter data for research coordinators and patients. This module allows coordinators and/or patients to intuitively enter study information.

  • Direct patient sign-on

  • Patient to-do lists

  • Automatic email notifications

  • Secure data collection

OPTIMIZE DATA MANAGEMENT

iMednet iMednet allows you to improve the efficiency of your tests, ensure the accuracy of your data and maximize resources with comprehensive data management modules for:

  • Making coding with ease and consistent

  • Randomizing easily

  • Streamlining inventory management and increasing

  • Automation of CEC allocation and risk

  • Rendre le codage facile et cohérent

Make coding easy and consistent

To improve efficiency, iMednet’s native coding module permit an automates coding and provides visibility to MedDRA or WHODrug data dictionaries. This allows users to easily create synonyms to optimize consistency between sites.

Randomize with ease

With iMednet Randomization you remove complexity and increase efficiency of the process, and contain study costs. Deploy simple and complex schemas with full blinding functionality, while also controlling when sites are able to perform randomization.

Streamlining inventory management and increasing

The optional iMednet module makes it easier to manage the inventory of research products

Automation of CEC adjudication and risk reduction

Simplify the CEC adjudication process and increase the visibility of individual adverse events with iMednet adjudication module.

TRIAL MANAGEMENT

Mednet’s trial management modules allow you to modernize your processes and more easily manage a wide range of clinical research in a unified platform.

Mednet's tools and native modules offer complete visibility and allow you to focus on important key tasks, such as :

  • CTMS

  • PAYMENT MANAGER

  • REPORTS MANAGER

  • RBM

  • DOCUMENT TRACKING

Focus on what matters most

You can customize the CTMS functionality. This allows you to manage and monitor the critical points of your study. iMednet allows you to effectively capture and manage movement checklists and easily track information at the site level. You can also manage the status of site document collection, training reports, site lists and more.

Take control of your site payments

iMednet Payment Manager allows you to enhance visibility, improve productivity and increase site approval when you modernize your clinical trials site payments. You can easily allocate site-specific budgets. And have the ability to view and approve eligible payments and access a complete transaction history on the same unified platform.

For real-time data insight access to robust reporting

You are able to quickly create unique reports in multiple formats with iMednet’s Report Manager.

Precise assessment of the potential risks of the study and future performance

A complete risk planning is provided by iMednet’s RBM module, that targeted SDV and visualization libraries.

Track IRB and other regulatory documents with ease

You increase visibility and effectively track documents such as IRB approval and renewal dates, IRB lists, IRB registrations and other regulatory documents in iMednet.

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