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What is ArcheMedX Ready?

ArcheMedX offers a solution designed for pharmaceutical and biotech trusts to enhance the effectiveness of their trial teams, streamline decision-making processes, and minimize delays in studies. By identifying the most capable sites and teams for conducting trials, organizations can sidestep common pitfalls that lead to study postponements. This approach not only cuts down on the time and expenses associated with problem resolution, particularly in the early phases of a trial, but also ensures that selected sites have a thorough understanding of patient eligibility criteria. Consequently, you can trust that they are better positioned to enroll suitable patients more efficiently, achieve enrollment goals, and reduce screen failure rates. Additionally, the trial team’s deep familiarity with the study protocol and its specific objectives fosters a comprehensive understanding of the project. This proactive strategy allows for the anticipation of potential risks, enabling teams to mitigate them effectively and ultimately resulting in fewer deviations throughout the trial process. Overall, this systematic preparation leads to a smoother and more successful trial execution.

What is Medable?

Medable provides a cutting-edge software platform tailored for the research and execution of clinical trials in a decentralized manner. This innovative technology is designed to engage patients remotely, ensuring the accuracy of data collection. Moreover, patients have the ability to give their consent for digital assessments from their own locations, while the platform adapts to various local languages and regulatory standards. You can optimize your protocol’s decentralization through our flexible, modular digital and decentralized clinical trial (DCT) platform, enabling extensive remote screening across the globe to meet your enrollment targets more efficiently. Create customized screening assessments that address your specific requirements, and improve the clarity of consent documents with responsive designs that work seamlessly on both web and mobile devices. Our remote eConsent experiences provide patients with a user-friendly interface akin to popular consumer applications. With our platform’s adaptability to local laws and languages, we ensure global flexibility to cater to a wide range of needs. By actively involving patients and minimizing the challenges tied to travel and scheduling for on-site visits, we significantly enhance patient access and engagement in the research study. This method not only streamlines the clinical research process but also emphasizes the importance of patient convenience and participation, ultimately fostering a more inclusive and effective research environment. In doing so, Medable redefines the way clinical trials are conducted, paving the way for a more patient-centered approach to medical research.

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

ArcheMedX

Date Founded

2013

Company Location

United States

Company Website

www.archemedx.com

Company Facts

Organization Name

Medable

Date Founded

2015

Company Location

United States

Company Website

www.medable.com

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

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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