ePRO Device Management

How It Works

Electronic patient-reported outcomes devices (ePRO devices) are mobile phones or tablets which gather patient-provided information about symptoms, side effects, drug reminders and other related questions during a clinical trial. It allows patients to answer questions and report on the well-being. 

ePRO devices are usually supplied to patients with preinstalled scripts or special apps which record subjects` responses or even photos or videos. Nowadays, while almost every fourth clinical trial involves ePRO, especially in trials with mental disorders and oncology, this fact proves that such a solution improves compliance and is a part of global trend on a patient centricity. 

This tool helps to track health behaviors and measure non-disease specific conditions both physical and emotional. In the meanwhile, you are planning to implement the ePRO solution in your clinical trial it is better to find the vendor in advance and to develop a strategy of further work. 

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About ePRO Device Management

In the meanwhile, you are planning to implement the ePRO solution in your clinical trial it is better to find the vendor in advance and to develop a strategy of further work. IRM can help you develop a user guide for you trial as well as to procure the sites with the set-up phones or tablets with the specific script or app. 

Our highly qualified partners are software providers who will manage the data storage and deployment which will be available to the monitors at any time. 

Our service merges both logistics and technology sides of the ePRO sourcing, having specialists onboard who manage procurement and delivery of the devices, scripts and apps installation, marking and labeling, and cloud-based software solutions. 

So if you need to remain patients committed to the protocol and to keep compliance on a high level please do not hesitate to contact IRM to obtain the consultation or proposal

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