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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.
Description
Only SAS offers a comprehensive, cloud-native environment for statistical computing in clinical research, featuring built-in analytic tools, adherence to data standards, and optional integrated analytic applications. This foundation enhances your capacity to modernize processes and expedite the introduction of new therapies into the market, ultimately contributing to improved health outcomes. By utilizing a collaborative platform, you can effectively manage and analyze information, streamline procedures, and provide trial results more efficiently to regulatory bodies. It serves as a unified solution for clinical analysis and submission, encompassing all necessary components for validation, compliance with regulations, version control, audit trails, and documentation assistance. The platform facilitates automation through customizable workflows, supports current and forthcoming integrations, and ensures the implementation and management of data standards and controlled terminology. Additionally, it features a central hub for all incoming data, automates data quality assessments, enhances data management practices, and prepares analytical data with greater accuracy, thus enabling more insightful outcomes. Ultimately, SAS equips clinical researchers with the tools needed to navigate the complexities of modern research and regulatory environments effectively.
API Access
Has API
API Access
Has API
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
Dassault Systèmes
Founded
1981
Country
France
Website
www.medidata.com/en/clinical-trial-products/unified-platform
Vendor Details
Company Name
SAS
Country
United States
Website
www.sas.com/en_us/software/life-science-analytics-framework.html
Product 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