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What is Gesund.ai?

Gesund represents the forefront of compliant AI manufacturing, focused on easing the market entry of clinically validated AI solutions. To adhere to regulatory requirements, our platform thoroughly audits and assesses third-party medical AI products to confirm their safety, efficacy, and impartiality. Gesund effectively oversees the complete AI/ML lifecycle for all stakeholders by integrating models, data, and expertise within a no-code interface that is user-friendly. We provide standardized, harmonized, and varied data designed to fulfill your machine learning needs as well as regulatory standards. By determining the validation requirements of models, Gesund.ai offers an ideal mix of high-quality data obtained from its vast network of clinical collaborators. Model developers can submit their clinical research to Gesund.ai to assemble the requisite datasets, after which they can upload their models onto Gesund.ai's federated validation platform, which can be deployed on-site at hospitals or in a secure private cloud. Each model is assessed using a validation dataset that is meticulously tailored at the hospital level, ensuring that the outcomes are both pertinent and trustworthy, thus improving the overall standard of healthcare innovations. In addition to fostering compliance, Gesund's holistic methodology significantly speeds up the implementation of effective AI solutions in medical environments, ultimately contributing to enhanced patient care and outcomes.

What is Biorce Aika?

Biorce's Aika is an innovative AI-powered clinical intelligence platform that revolutionizes the clinical trial lifecycle by converting labor-intensive processes for protocol creation and feasibility assessments into streamlined, evidence-based automation. Drawing on insights from nearly one million real-world trials, Aika can rapidly generate initial study protocols, detailed regulatory documents, site feasibility assessments, risk management plans, and other essential components of trials much quicker than traditional methods, thus reducing the likelihood of delays and costly revisions. This platform promotes complete transparency in its recommendation processes, empowering teams to confidently convey their decisions to regulatory bodies while ensuring expert supervision remains intact. Furthermore, Aika effectively marries the rapid efficiency of AI with deep clinical expertise, significantly shortening trial preparation durations from weeks to just days, which minimizes amendment risks and overall project vulnerabilities. By integrating seamlessly into current workflows without necessitating extensive retraining, Aika allows clinical trial teams to prioritize strategic decision-making over tedious administrative responsibilities. As a result, the focus shifts towards enhancing trial outcomes and optimizing resource allocation, ultimately driving innovation in clinical research practices.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Gesund.ai

Company Location

United States

Company Website

www.gesund.ai/

Company Facts

Organization Name

Biorce

Date Founded

2024

Company Location

Spain

Company Website

www.biorce.com/our-software

Categories and Features

Categories and Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

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