This tool makes easy work of creating your eCRF. You can use a comprehensive set of variables and options to quickly set up your questionnaires and datasets, embed your validations, and check the data input in the Test mode.
Our randomisation tool simplifies the use of randomisation methods, such as (random) block randomisation, simple randomisation, or minimisation. The tool allows the definition of simple and complex randomisation arms and stratification classes.
Patient Self Service enables separate schedules for sending individual questionnaires so that patients can complete questionnaires online securely, and from any location. One clear overview provides access to both responses and progress.
This tool can be used to set notifications for various events within the research study, fully automating the process when an SAE, SUSAR or SADE is logged.
Are you looking to import or link information from external sources and files? This service makes it possible to import (un)structured data from various sources directly into Data Management, as well as export research data to various file formats such as Excel and SPSS.
The Stock Management tool can be used to manage, log, and issue medicinal products or devices. It provides an immediate overview of the up-to-date stock for each site and sends automatic notifications when stocks need to be replenished. The Stock Management tool can be linked to the Randomisation tool.
This service can be used to search (un)structured data (free text fields) for patient populations based on inclusion parameters. The populations detected – along with associated data – are easily transferred to the eCRF.
We can help you use algorithms to predict certain outcomes based on existing data. These models can also be used to verify whether you are collecting the right data to formulate an answer to the research question.
The Research Manager Research Platform is suitable for both Multi-centre and Single-centre studies. Collecting research data for separate sites is very straightforward, with each participating centre having access to the study file to view the status of the local feasibility per site at any time. The sites can collaborate securely, yet they work separately by managing the various roles and authorisations.
This service provides a library containing an extensive database of validated questionnaires. These questionnaires can now be used in any study, saving a significant amount of time when establishing the eCRF and reducing the risk of errors.
Our consultants can help you with the design of your eCRFs as well as support your research setup, data collection, and study management.
Places the patient front and centre. Which personally identifiable information has your patient given consent for? This service supports the implementation of a patient journey that involves the collection of relevant data aimed at the patient’s perspective.
All data are stored in accordance with the FAIR principle so that it can be exchanged with any system, making existing data more accessible to researchers.
Increasingly stricter legislation and regulations mean that audit trails are essential. Our audit trails record all procedures and amendments for each user and each patient, ensuring your compliance without the need for further administrative burdens.
We zijn altijd bereid met je mee te denken over wat voor jou de beste oplossing is. Misschien wil je onze oplossing eerst even uitproberen? Alles is mogelijk. Je hoeft alleen maar het contactformulier aan de rechterkant in te vullen. Je kunt ons ook altijd even een mail sturen.
Blijf op de hoogte!