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e-novex provides electronic data tools that change medical research

Our expertise helps you in setting-up your database or in transferring data, on time, on budget

To be used in a variety of trials including investigator initiated or First In Human trials

To be used in a variety of trials including investigator initiated or First In Human trials

Stay in charge of your budget

Stay in charge of your budget

Create your own eCRF

Create your own eCRF

Manage your imaging logistics in real-time

Manage your imaging logistics in real-time

Online tracking and communication keeping everybody informed

Online tracking and communication keeping everybody informed

Transferring your data without any installation requirements

Transferring your data without any installation requirements

Flexible eCRF for approval studies including pivotal or IDE

Flexible eCRF for approval studies including pivotal or IDE

Facilitating communication inside and outside the eCRF

Facilitating communication inside and outside the eCRF

Stay in charge of your data by creating your own data exports

Stay in charge of your data by creating your own data exports

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May 8, 2014 | Ghent, BELGIUM

Knowledge For Growth

May 20-23, 2014 | Paris, FRANCE

EuroPCR

June 17-18, 2014 | Maastricht, Netherlands

Biomedica 2014

July 30-August 3, 2014 | Orlando, United States

International Spine Intervention Society

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  • Today our project team received the following feedback: “Your support is awesome, there is always an immediate follow up of any question I may have. Great!” Try them also by using e-capture.net, the Core Lab Tracker or edc2go.

    17 February, 2014 15:21
  • The FDA issued a final rule entitled “Medical Device Reporting: Electronic Submission Requirements,” revising its postmarket medical device reporting regulation and making technical corrections. The rule also identifies changes to the content collected on the Form FDA 3500A. http://lnkd.in/drWsE5V less

    17 February, 2014 08:27
  • e-capture.net is used by 6,167 active users in 58 countries. An amazing number of persons using this e-tool for their regulatory and often complex studies. The tool allows you to upload source data, create flexible exports and provides an easy overview of the possible action items.

    11 February, 2014 14:21