We provide a digital solution to make your product safer, acquire real time (pharmaco)vigilance data and to connect all crucial stakeholders.
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• Easy implementation of post-approval safety studies, registries and treatment follow ups
• Make use of a ‘Virtual (Pharmaco)vigilance Clinic’ to digitally connect with experts
• Increase the safety of your product through early detection of adverse events – real world, real time

• for thorough processing and correct interpretation of adverse events and reduction of uncontrolled spontaneous reports
• to give rapid support for the patient
• to support regulatory reporting

Decentral data plays an increasingly important role for clinical studies. Our clinical study platform enables decentral data collection and conduct of your study still allowing the responsible trial team to keep the full overview - for real world analyses, register studies and clinical trials.
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1. Digital Visits - we support the collection of all relevant data and digital biomarker from the patient for your clinical research - with data analysis in real time:‍

• Patient-reported outcomes
• Clinician-reported outcomes
• Remote patient monitoring with wearables, smartphones and devices
• Patients can be provided with all relevant information to understand and follow the clinical study
• Bi-directional communication between study participant and trial team is supported by a chat function and telemedicine

2. Digital Trial Organization - to reduce trial protocol violations and increase trial quality:

We connect all parties involved in the conduct of the clinical study: patient, study team, CRO, sponsor and guide them through the visits and the protocol. Everyone knows when, where and what!