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What is SiteCentric?

SiteCentric is a comprehensive platform tailored specifically for clinical trial management, developed by research sites to meet their distinct requirements, integrating multiple functions like CRM, eISF, CTMS, financial oversight, and reporting into a single, cohesive solution. This all-encompassing tool simplifies and automates various processes throughout the entire lifecycle of a clinical trial, enabling effective management of study leads and the organization of pipeline activities through its specialized CRM system. Essential documents, such as budgets, contracts, eReg, training records, and source documentation, are centralized to streamline the startup process. Moreover, the platform boosts enrollment initiatives through strategic outreach and taps into existing databases for enhanced recruitment efficiency. Patient visits are meticulously tracked, ensuring high-quality eSource data is captured, while internal quality control checks, version control, and audit-ready eISF documentation are consistently maintained. Financial management is also a key feature, as it oversees aspects like budgets, invoicing, payment reconciliation, and patient reimbursements. The inclusion of leadership dashboards presents crucial performance metrics and trends in real-time, enabling research sites to make swift, informed decisions. Overall, SiteCentric significantly enhances clinical trial operations by consolidating various functionalities into a single, efficient platform, ultimately empowering research sites to achieve their goals more effectively while improving collaboration and operational efficiency.

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.

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

SiteCentric

Date Founded

2022

Company Location

United States

Company Website

sitecentric.com

Company Facts

Organization Name

ArcheMedX

Date Founded

2013

Company Location

United States

Company Website

www.archemedx.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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