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ease
features
design
support

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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

Germany leads the way in research across Europe, conducting over 600 clinical and non-clinical studies each year. Managing these studies is becoming more intricate, as it requires careful coordination of appointments and staff, timely updates of study data, and easy access to documents for inquiries. It’s time to eliminate the burdens of a paper-based system; by switching to a lightweight tablet, you can locate information within seconds and dedicate your precious time to what truly matters: advancing your research. The digital study management solution from studioMED+ is designed to support you in this transition. Regardless of your location or the time, studioMED+ offers a versatile tool that seamlessly adapts to your specific needs, ensuring that your research process is efficient and effective. Embrace the future of study management and enhance your productivity with this innovative solution.

API Access

Has API

API Access

Has API

Screenshots View All

Screenshots View All

Integrations

BioGRID
ClinVigilant
Datavant
Rave CTMS
Rave EDC

Integrations

BioGRID
ClinVigilant
Datavant
Rave CTMS
Rave EDC

Pricing Details

No price information available.
Free Trial
Free Version

Pricing Details

$200 per month
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

studio.201 software

Founded

2019

Country

Germany

Website

www.studiomedplus.de

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

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

Alternatives

Alternatives

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