As a professional in the pharmaceutical industry regulations require the strict management of any clinical trial. Protocols are to be followed very strictly, and audit trail and monitoring are crucial. Imagine handling all tasks and operations – from recruiting and communication with participants to correctly storing sensitive data – in one system.
Let EasyTrial.net help decentralise your clinical trials
By digitising traditional clinical trials you will achieve a more cost-effective and time-saving management of your studies.
The use of digital solutions and health technologies in part or during the entire trial process – from patient recruitment, participant information, obtaining informed consent forms, clinical site visits, trial procedures, sampling, medication administration and safety monitoring – enables the more effective conduct of the trial.
Secure great hit-rate and high participant engagement
The use of online platforms and social media for the recruitment of trial participants entails global recruitment of trial patients and recruitments of patients who do not normally have the time and opportunity to participate in clinical trials. It can e.g. be patients with chronic or rare diseases, disabilities that make transportation difficult or patients with full-time work and/or children who require presence in the home.
Use EasyTrial.net to screen patients by answering questionnaires or online tests before entering the study. Follow up by making sure the participants understand the participant information before signing the informed consent form using e.g. NemID or e-Boks in Denmark.
Drop site visits and e-diaries, electronic patient-reported results, and data collection from fitness devices, mobile apps, wearables, IoT (internet of things) and digital watches.
Instead ensure full online control in your trial management by letting EasyTrial.net handle the transfer of large amounts of sensitive health data over the internet with our highly secure and approved clinical trial management system.
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