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What is YPrime?

The merging of eCOA with digital technology is revolutionizing the landscape of clinical research, creating a bridge between conventional practices and cutting-edge, patient-focused methodologies. Opt for YPrime's eCOA solutions to secure not only superior patient data but also to improve the overall experience for sponsors, investigator sites, and patients. Utilizing a versatile software development approach, YPrime can rapidly customize and modify features to align with specific study needs within a remarkable 8 to 12-week timeframe. Our dynamic and visually appealing design process enables clients to assess the system at different phases of development, keeping them well-informed prior to the system's launch. Moreover, our pre-validated and adaptable authoring environment not only expedites startup timelines but also allows for modifications after production, such as protocol changes, thereby becoming an essential resource for clinical research. This dedication to flexibility and responsiveness solidifies YPrime's status as a frontrunner in the changing world of clinical trials, ensuring that we remain at the forefront of innovation in the field. In doing so, we strive to enhance the efficiency and effectiveness of clinical studies, ultimately benefiting all stakeholders involved.

What is RegDoc eSafe?

Introducing an eReg platform designed specifically for study sites, this solution guarantees swift setup without enforcing strict workflows, featuring a user-friendly interface and capabilities. You can try RegDoc eSafe at no cost today! This platform serves as a secure repository for source documents and comes with tools that enable the transfer, redaction, and assignment of time-limited, role-based access to sensitive data. RegDoc eSafe offers rapid and adaptable configuration options, requires little training for easy navigation, and includes a thorough yet efficient validation procedure. The implementation process is streamlined to quickly ready your clinical study sites for operation, and regulatory binder templates are conveniently accessible within your site for easy retrieval. The platform supports user uploads and has access control settings, supplemented by dedicated training sessions for both administrators and users. MedPoint emphasizes compliance, assisting you in all necessary steps to validate our software successfully. With extensive experience in developing and maintaining validated systems, MedPoint is subject to regular audits by study sponsors, which ensures the highest reliability and quality in our services. Our ongoing commitment to improvement and user satisfaction not only distinguishes us in the industry but also reinforces our dedication to providing exceptional support. Furthermore, we continuously seek feedback from our users to enhance the platform further, ensuring that it meets evolving needs in the field.

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

YPrime

Date Founded

2006

Company Location

United States

Company Website

www.yprime.com/ecoa/

Company Facts

Organization Name

MedPoint Digital

Company Location

United States

Company Website

www.medpt.com/site-services/

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

Electronic Data Capture

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

Categories and Features

Document Control

Archiving & Retention
Automated Routing
Change Management
Compliance Management
Electronic Signature
Escalation Management
Periodic Review
Version Control

Document Management

Access Controls
Archiving & Retention
Collaboration Tools
Compliance Tracking
Document Archiving
Document Assembly
Document Capture
Document Conversion
Document Delivery
Document Indexing
Document Retention
Electronic Signature
Email Management
File Recovery
File Type Conversion
Forms Management
Full Text Search
Offline Access
Optical Character Recognition
Print Management
Version Control

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