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About EvidentIQ eConsent

EvidentIQ eConsent is an electronic consent management platform from EvidentIQ that supports clinical trial processes. It provides features such as remote patient engagement, informed consent tracking, and document management so researchers can simplify participant onboarding and compliance. The platform allows for real-time updates and easy access to consent documents, ensuring patients have a clear understanding of their participation. Designed with regulatory compliance in mind, it facilitates documentation and audit trails necessary for clinical studies. Key capabilities: remote patient engagement informed consent tracking document management regulatory compliance real-time updates Best for: clinical trial professionals that need efficient management of patient consent processes.

EvidentIQ eConsent Details

Vendor
EvidentIQ
Year Launched
2021
Location
Rathausmarkt 5, 20095 Hamburg, Germany.
Deployment
cloud
Training Options
documentation, videos, live online, in person
Countries Served
All Countries
Languages
English, Spanish, French, German, Italian, Portuguese
Users
Clinical Trial Coordinators, Research Investigators, Data Managers, Ethics Committee Members, Regulatory Affairs Professionals
Industries Served
Healthcare, Clinical Research, Pharmaceuticals, Biotechnology, Life Sciences
Tags
eConsent, clinical trials, patient engagement, digital consent, healthcare software, pharmaceutical software, electronic informed consent.

EvidentIQ eConsent's In-App Market Place

Does EvidentIQ eConsent have an in-app market place?

Yes

How many Mini-Apps in the marketplace?

0

Mini Apps

Pricing Options

Free trial
Free version
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Accepted Payment Currencies

USD ($), EUR (€), GBP (£), AUD (A$), JPY (¥), CAD (C$), CHF (CHF), CNY (¥), SEK (kr), NZD (NZ$), INR (₹), SGD (S$), HKD (HK$), KRW (₩), NOK (kr), MXN (Mex$)

Pros & Cons

  • Enhanced Patient Engagement: Multimedia features improve patient understanding and engagement.
  • Regulatory Compliance: Adheres to industry standards, ensuring secure and compliant consent processes.
  • Remote Accessibility: Facilitates remote participation, accommodating diverse patient needs.
  • Streamlined Processes: Digitizes the consent process, reducing administrative burden.
  • Comprehensive Support: Offers various support channels, including email, phone, and a knowledge base.
  • Regulatory Complexity: Compliance with different regional laws can be challenging.
  • 8. Internet Dependency: Requires a stable internet connection for full functionality.
  • 9. Limited Customization: May not be highly flexible for unique clinical trial needs.
  • 10. Support Availability: No mention of 24/7 live chat support.

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