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 With increasing pressure on companies to prove their products'
commercial value and long-term safety, late phase studies have
never been more important. However, such studies bring particular
challenges for ePRO data collection.
For example, retaining patients for the entire duration of a trial can be
a challenge, while the logistics of managing the large number of
sites and subjects inherent to late phase trials can be operationally
burdensome. When combined with their relatively low budgets,
it's clear such challenges require a specialized solution for ePRO
data collection – TrialMax Web™.
The success of a late phase study hinges on a positive patient
experience. That's why we've developed a fully customizable,
globally integrated, online portal that uses engaging and user friendly
interfaces to collect and collate high-quality ePRO data.
Developed especially with late phase trials in mind (and with
input from leading scientists and therapeutic experts), TrialMax
Web™ aids retention, ensures compliance and delivers data of
the highest scientific integrity – quite simply, TrialMax Web™ is a
revolution in ePRO data collection.
TrialMax Web™ revolutionizes patients' late phase study experience
through motivating
and reminding features, such as:
- Today's activities reminders – reminds patients of their
daily tasks
- Study information – provides easy-to-understand study
information
- Study events timelines – allows patients to better
incorporate the study schedule into their lives
- SMS and email reminders – ensures patients remember
important study dates and milestones
- Rewards for compliance – gives patients immediate
feedback and rewards for a job well done
And because we know every study is different, these tools are
both fully customizable and fully configurable, enabling you to
tailor your ePRO strategy to your trial's needs.
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