Why invivodata
“I have used eDiary products from a variety of vendors and invivodata has the best overall package.”
Vickie Lassak
Clinical Research Coordinator, Allegheny Pain Management
Why invivodata > Site Benefits
Site Benefits
Ensuring that investigative site staff are productive and effective is critical to the success of any clinical trial – especially those involving ePRO data. They require the highest quality support, tools, and processes to ensure that all aspects of the ePRO trial run smoothly.
No one has more experience in providing practical ePRO solutions and support services to investigative site staff than invivodata. In addition to providing the industry’s most comprehensive training and support services, we are continually developing new study tools that minimize any burden on clinical research coordinators and enable them to run your ePRO trials efficiently. Examples of the benefits provided to sites:
- Intuitive ePRO Patient Management: invivodata’s EPX™ system provides clear views into ePRO trial data and information they need to successfully manage clinical studies involving invivodata’s ePRO solutions. With EPX, sites can:
- easily access real-time patient data
- monitor and manage patient compliance between visits
- process data clarification forms online through the EPX eDCF process, eliminating time-consuming and often misplaced paper faxes.
- Space-saving Device Charging: Device charging used to be a burden, since all devices needed to be
plugged into power strips using individual AC adapters. To reduce this burden, invivodata developed the EasyCharge™ connector that simultaneously charges up to eight DiaryPRO devices with a single cable.
- Integrated Training System: invivodata's solutions eliminate the need to label and manage multiple devices for training and patient use. We integrate a training mode into every diary we create for easier device administration.
- Single System to View Integrated EDC and ePRO Data: ePRO data captured on DiaryPRO can be integrated into Medidata’s Rave® eClinical data management platform and be viewed within a single system. The integration gives study sites rapid access to trial data so that site personnel can actively monitor subjects’ behavior and take proactive measures to improve their compliance with the protocol without having to log into different eClinical interfaces.
- Streamlined Device Management: invivodata has developed organizational and space saving packaging for DiaryPRO patient and site kits, making it easier to store, charge, assign, and return the trial equipment.
invivodata is committed to continually delivering the most practical tools and processes that will help investigative site personnel manage ePRO studies with minimal impact on their additional duties within the course of a clinical study. We routinely conduct surveys of site personnel during and after ePRO studies to better understand their challenges and how we can help address them.
To learn more about invivodata's site-focused solutions, contact us today.