Study & Form designer

Create your study design, all workflows, rules and forms with our intuitve online tool. You can control the whole process yourself. We help, where every you need a hand. Extensive options for importing and exporting data sets help you to use existing code lists, variables or translations.

ODM Compatible

An ODM (Operational Data Module) is a clinical data management system standard. This forms the baseline of our Case Report Forms (CRFs). Where there are large capacities of heterogeneous, linked data the CDISC ODM data model forms the scaffolding required to initially capture, and subsequently and re-use data. Data saved in this format can be integrated into our system from existing trials, as well as forwarded into other systems of data capture, where necessary.

Tailored Design

Assuring the visual identity of your EDC:

As every trial is unique, so is the interface which it is built upon. From the visits, questions, forms, layout and even colour scheme, all of the features of cvEDC are entirely customizable. Even after the interface is in production, users can move around features in which suit them best, according to their needs. We assure that users have the best possible experience in managing their clinical data.

Monitoring

Our EDC system offers you extensive monitoring options for verifying the source data. No matter if you want to check samples or 100%.

Target Data Views

See the trees from the forest!

Data from clinical trials is extensive, with the inclusion of demographic data, clinical history, and trial outcomes present for every patient – in trials which can contain thousands of patients. We strive to make all of this data as clear and searchable as possible. Patients can be assorted according to any variable which might define them, including multiple factor searches – giving view only to a specific demographic which may be of interest to you and your research. Additionally, all of our trial events, forms and queries are also based on intuitive designs and patterns which make sense in the context of immense data capture.

Input / Output

cvEDC is capable of incorporating any data you may be carrying across from a previous trial, or from your clinic. Data can be input quickly from any of the standard formats of clinical data management (such as CVS and excel formats) All of the data which is input into the trial can be exported into a variety of formats for your research requirements, including all standards, such as CSV and Excel, as well as software specific formats for SPSS and STATA.

External Resources

External, regularly updated lists from well known sources:

A feature we provide within our system is the possibility of integrating existing clinical terminology databases to support the collection of trial data. Lots of medical issues – such as comorbidities of patients in your trial – can come from well-known and regularly maintained databases, such as ICD 10. Drugs and concomitant medications can come from MedDRA or Rote Liste. We aim to improve the quality of data collected, whilst making it easier for participating centres to input the correct variables where required. Therefore all of the data in these databases is searchable and indexed – and can autocomplete.

Responsivness

cvEDC is entirely browser-based and can be viewed on any device with a browser. There is no installation required, no administrative access necessary for the use of cvEDC on network computers - just log in and work. The interface is responsive and works in a way which assures maximum readability and usability on any device – irrelevant of the screen size.