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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.

What is Longboat?

Longboat is a cloud-based platform tailored to enhance the efficiency of clinical trials, featuring an integrated Guided Compliance toolset that provides ongoing assistance to users throughout the entire process. By equipping clinical trial site personnel with vital resources, Longboat allows them to focus more on patient care. Moreover, participants can conveniently access important study information and receive timely reminders for upcoming visits. The system streamlines the management of protocol amendments, ensuring they are implemented smoothly and effectively. Additionally, Longboat centralizes the secure exchange of regulated documents among sponsors, CROs, and sites, thereby significantly improving the startup process and alleviating the burden of traditionally tedious tasks for all involved in research. With a unified support platform, all primary stakeholders—including clinical operations teams, monitors, site staff, and trial participants—can access tailored content that meets their specific needs. This holistic strategy guarantees that site staff are well-equipped with the necessary tools and resources to stay engaged and compliant while maintaining a strong focus on participant welfare. In this manner, Longboat not only enhances operational efficiency but also significantly enriches the overall experience for everyone participating in the clinical trial, fostering a more collaborative and effective research environment. By prioritizing user needs, Longboat paves the way for innovative solutions in clinical research management.

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

MedPoint Digital

Company Location

United States

Company Website

www.medpt.com/site-services/

Company Facts

Organization Name

Advarra

Date Founded

1993

Company Location

United States

Company Website

www.advarra.com/solutions-for/sponsors-cros/longboat-platform/

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

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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