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Enhanced Patient-Reported Experience
electronic Patient-Reported Outcomes
Discover the numerous benefits of modern and effective participant engagement with ePRO. This allows clinical research participants to actively participate in their own care, providing researchers with valuable insights while enhancing the quality of results and the study.
Increased Engagement Among Clinical Research Participants
ResearchManager ePRO makes it easy for clinical research participants to capture their input directly in the secure Clinical Research Suite. They can fill out questionnaires on their own devices, such as laptops, mobile phones, and tablets. This increases the accessibility of the research and user-friendliness, while simultaneously improving the quality of research data.
Data Collection and Automated Schedules
With ePRO, automated schedules can be set up for sending questionnaires. Schedules can be configured to send questionnaires at specific times—such as weekly, monthly, or after a specific treatment event. Triggers and reminders can be set to ensure that patients do not miss questionnaires. Manual scheduling and sending reminders are thus a thing of the past, guaranteeing consistent data collection.
Seamless Data Integrity: Error-Free and Consistency
One of the key advantages of ePRO is the significant improvement in data quality. Manual data entry can lead to errors, delays, and inconsistencies. With ePRO, data is captured electronically directly by patients, significantly reducing the chances of human error. Additionally, built-in validations and checks ensure that the entered data is accurate.
20%
Higher response rate
Improves response rates compared to paper surveys.
30%
Higher engagement
Boosts patient involvement with intuitive interfaces and reminders.
35%
Faster data collection
Reduces collection time with real-time data entry.
Highlighted features
Real-Time Data Capture
Collect patient-reported outcomes in real-time, ensuring up-to-date and accurate data.
Seamless Customization
Design custom forms tailored to study needs, create personalized email templates for streamlined communication, and brand the ePRO tool with logos for a professional and consistent appearance for study participants.
Automated Scheduling and Reminders
Automatically schedule assessments and set up reminders to prompt patients to complete their tasks, improving response rates.
Multi-Device Accessibility
Accessible on various devices, including smartphones, tablets, and computers, offering flexibility for study participants.
Audit Trail
Complete audit trail functionality to document all modifications to the data, including the user who made the change, the timestamp of the change, and a detailed description of the alteration.
Users and Partners of ResearchManager
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Discover why our users have chosen ResearchManager
All-in-one suite for every stage of clinical research
The Clinical Research Suite (CRS) is an all-in-one solution for managing Clinical Data and Operations, from trial planning to completion. CRS provides a cost-effective solution by combining multiple tools and services into one platform, reducing the need for multiple vendors.
Scalable Solutions for Organizations of All Sizes
The Clinical Research Suite scales to meet the needs of any organization. Small organizations can choose the Pay-as-you-go On Demand model, while mid-size and large organizations benefit from the Enterprise package with structured plans for multiple ongoing studies, ensuring efficient resource management and growth.
Fast-go live within 5 working days
The Clinical Research Suite (CRS) offers a fast go-live option within 5 working days. Additionally, fully customized implementations are available, tailored to specific needs, ensuring the platform aligns perfectly with trial requirements.
Dedicated team with personalized support
Experienced in-house second-line assistance and a dedicated account manager are always included to ensure seamless operations and personalized guidance throughout the entire process.
Proven success
With over 20,000 studies conducted, 8,000+ active users, and more than 1,000,000 patients enrolled, ResearchManager’s Clinical Research Suite (CRS) has a proven track record of delivering successful clinical trials worldwide.
Compliance and Technical Information
ResearchManager is compliant
- Offices in the Netherlands (HQ) and in the USA.
- ISO 27001 certified
- NEN 7510 certified
- ISO 14155 compliant
- 21 CFR PART 11 compliant
- GCP compliant
- GDPR compliant
- HIPAA compliant
- Secure connection with Comodo’s EV SSL certificate
Data Centers and Cloud Services
1) Data Centers in the EU
- TIER 3+
- SOC 2 security standards
- ISO 9001 certified
- ISO 14155 certified
- ISO 27001 certified
- NEN 7510 certified
- Dedicated backup server, AES 256 encrypted
2) Regional Cloud Services
ResearchManager provides localized cloud services in various regions (e.g., USA, Canada, Australia, UK, Japan), ensuring compliance with regional data residency regulations. This guarantees that data is stored and processed within the respective country’s jurisdiction, adhering to local security and compliance standards.
Saskia van Gastel
Accountmanager
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