Overview
Florence eConsent is an advanced electronic informed consent solution designed specifically for clinical trials. It simplifies the process of obtaining participant consent by providing secure, efficient, and fully digital workflows. This platform ensures that both researchers and participants can easily manage consent forms, enhancing the overall efficiency of clinical studies. By digitizing every document and automating workflows, Florence eConsent centralizes data, accelerates operations, and boosts team capacity. This not only streamlines the research workflow but also enhances productivity and ensures compliance with regulatory standards.
Highlights
- Simplify and accelerate the consent process with secure, paperless workflows.
- Easily manage and track consent forms across studies in one compliant platform.
- Improve team productivity while meeting regulatory standards like 21 CFR Part 11.
Details
Introducing multi-product solutions
You can now purchase comprehensive solutions tailored to use cases and industries.
Features and programs
Financing for AWS Marketplace purchases
Pricing
Dimension | Description | Cost/12 months |
|---|---|---|
Annual Commitment | Starter Pack | $30,000.00 |
The following dimensions are not included in the contract terms, which will be charged based on your usage.
Dimension | Description | Cost/unit |
|---|---|---|
Active Study Site | Customer's active Study-Site count for subscription fee per month | $125.00 |
Vendor refund policy
All fees are non-cancellable and non-refundable except as required by law.
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Delivery details
Software as a Service (SaaS)
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Vendor support
For support inquiries, please reach out to our customer service at support@florencehc.com or visit our support page at
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