Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
H1 is an international company specializing in healthcare data technology, offering a robust platform that provides in-depth insights into the healthcare sector by analyzing data from more than 11 million healthcare professionals. The solutions provided by H1 are tailored to enhance the effectiveness of medical affairs, clinical trials, and commercial teams by supplying immediate access to healthcare professional insights and AI-driven analytics, which ultimately lead to meaningful interactions and expedite the process of developing and distributing life-saving therapies. With an expansive database that features over 160 million peer-reviewed articles, 350,000 clinical trials, and 8 billion medical claims, clients can pinpoint key opinion leaders, streamline the selection of clinical trial sites, and connect with suitable prescribers to guarantee that patients obtain the correct treatments. Moreover, H1 ensures that organizations can comply with risk, compliance, and disclosure standards effortlessly. Every action taken is meticulously captured in real-time activity logs, enhancing transparency and accountability within the platform. This commitment to comprehensive data management empowers healthcare professionals to make informed decisions that positively impact patient outcomes.
Description
The Medidata Clinical Cloud represents our innovative platform designed to revolutionize the clinical trial journey for patients, sponsors, CROs, and research institutions. As the sole comprehensive technology solution focused exclusively on clinical research, the Medidata Clinical Cloud addresses the entire research spectrum from inception to completion. Our platform enables organizations in the life sciences and medical device sectors to reduce development expenses, manage risks effectively, and expedite the introduction of treatments and devices to the marketplace. Whatever selection you make for your clinical trial initiatives, you will benefit from the capabilities of the Medidata Clinical Cloud. At Medidata, we are at the forefront of the digital evolution in clinical research. With the power of artificial intelligence, machine learning, and sophisticated analytics, our platform connects researchers, study coordinators, investigators, and patients, thereby hastening the research process. Additionally, it provides a regulatory-compliant, patient-friendly electronic informed consent solution for clinical trials, ensuring a smoother experience for all parties involved. This integration of advanced technology not only streamlines operations but also enhances the overall quality of clinical research.
API Access
Has API
No
API Access
Has API
No
Integrations
BioGRID
No
ClinVigilant
No
Datavant
No
Greenlight Guru Clinical
No
Rave CTMS
No
Rave EDC
No
Integrations
BioGRID
Yes
ClinVigilant
Yes
Datavant
Yes
Greenlight Guru Clinical
Yes
Rave CTMS
Yes
Rave EDC
Yes
Pricing Details
$500 per deal
Free Trial
No
Free Version
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
Live Rep (24/7)
Yes
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
Yes
In Person
Yes
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
No
In Person
Yes
Vendor Details
Company Name
H1
Founded
2017
Country
United States
Website
h1.io
Vendor Details
Company Name
Dassault Systèmes
Founded
1981
Country
France
Website
www.medidata.com/en/clinical-trial-products/unified-platform
Product Features
Virtual Data Room
Anonymity Management
No
Audit Trail
No
Collaboration
No
Data Protection
No
Data Storage Management
No
Document Tagging
No
Due Diligence Management
No
Procurement Management
No
Project Management
No
Role-Based Permissions
No
Secure Preview
No
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
No
Document Management
No
Electronic Data Capture
No
Enrollment Management
No
HIPAA Compliant
No
Monitoring
No
Patient Database
No
Recruiting Management
No
Scheduling
No
Study Planning
No