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Monitoring adverse effects

Monitoring adverse effects is an essential part of clinical pharmaceutical trials and the registration process for new pharmaceuticals. Enabling patients to be contacted fast and efficiently through automatic text messages, the service allows cost-effective monitoring of adverse effects. The service also significantly reduces the workload of research centers workload and makes it possible to complete trials on schedule.

The service is pleasant and easy to use for patients, thereby improving compliance in clinical pharmaceutical trials. As the number of patients grows, the benefits of the service increase as well.

Monitoring adverse effects
In this example patients are asked for possible drug-related adverse effects in a phase IV trial. Patients can respond easily with their own mobile phone.

Monitoring adverse effects

The service draws graphs by study and therapy area. This example graph illustrates adverse effects during the trial.