Protocol Manager logo

Protocol Manager

by Atlant Systems · Since 2010
No reviews yet
ActiveAvailable globallyCloud
Quick facts
VendorAtlant Systems
Year launched2010
StatusActive
LocationWilmington, Massachusetts
Countries servedGlobal
Languages7
Integrations1+
Free tierN/A
Free trialN/A
Contact salesYES

About Protocol Manager

Protocol Manager is a software platform from Atlant Systems that provides comprehensive management of protocol-related activities. It includes features such as a Privacy Statement, Trademarks functionality, and a Mission overview, so users can easily navigate legal and compliance requirements. Additionally, Protocol Manager offers insights into adWATCH - AE and adWATCH - CAPA, which assist with advertising management and compliance tracking. The platform supports organizations in maintaining adherence to regulations while managing their operational protocols effectively. Key capabilities: Privacy Statement Trademarks functionality Mission overview adWATCH AE adWATCH CAPA Best for: organizations that need to manage and comply with protocol regulations effectively.

Protocol Manager, developed by Atlant Systems, is a comprehensive Clinical Trial Management System (CTMS) that supports the management of global clinical trials across various phases of development, including drugs, devices, biologics, and vaccines. This off-the-shelf, configurable platform offers a wide range of features designed to streamline clinical operations, ensuring compliance, and enhancing efficiency in clinical trials. Although information on the user interface and specific design elements is somewhat limited, Protocol Manager is noted for its flexibility and ease of use, which are integral for simplifying complex trial management tasks. The platform's ability to automate various processes, such as investigator payments, site contracts, and tracking subject visits, ensures consistency and reduces manual errors across multiple trials. One of the key advantages of Protocol Manager is its robust trial tracking and database functionalities, which allow for the effective management of crucial trial information, such as documents, payments, inventory, and monitoring visits. The system also supports real-time site portals, which facilitate smooth communication and collaboration with trial sites.

Pros & Cons

Pros
  • Supports on-line and off-line use, enhancing flexibility.
  • Integration with EDC and IVRS systems for seamless data handling.
  • Templates for ease of use and efficiency.
  • Real-time site portal for efficient trial management.
  • Strong focus on investigator payments and financial management.
  • Wide range of reporting options for better trial insights.
Cons
  • Not an Electronic Data Capture (EDC) or Clinical Data Management System (CDMS).
  • May require significant configuration to suit specific company needs.
  • Limited information on user interface design or ease of use.
  • Integration with non-Web Services systems requires manual export/import.
  • No clear pricing available.
  • May require external systems for certain trial management tasks.

Features

Key features

Full-Scope CTMS

Manages all aspects of clinical trials.

Configurable and Off-the-Shelf

Adaptable to specific needs while readily available for use.

Supports Global Trials

Designed for managing international trials of drugs, devices, biologics, and vaccines.

21 CFR Part 11 Compliance

Aids in achieving compliance with FDA regulations.

Tracking and Database

Provides a robust system for tracking trial information and metrics.

Automation and Consistency

Automates tasks and ensures consistency across trials.

Wide Range of Reporting Options

Offers various reporting capabilities.

Metric Measurements

Tracks and measures key performance indicators.

Investigator Payments

Manages investigator payments.

Site Contract and Payment Management

Handles site contracts and payments.

Real-time Site Portal

Provides sites with real-time access to relevant information.

Time & Expense Reporting

Tracks time and expenses associated with trials.

CTMS/EDC/IVRS Integration

Integrates with EDC and IVRS systems via Web Services or export/import.

On-line and Off-line Use

Allows for both online and offline access.

Hosted and/or Licensed Use

Offers flexible deployment options.

Email Alerts

Provides email alerts for important events.

Industry Standard Security

Incorporates security measures to protect data.

Templates

Offers templates for ease of use and efficiency.

Business Development Module

Includes a module for business development activities.

Additional features

Full-Scope CTMS

Manages all aspects of clinical trials.

Configurable and Off-the-Shelf

Adaptable to specific needs while readily available for use.

Supports Global Trials

Designed for managing international trials of drugs, devices, biologics, and vaccines.

21 CFR Part 11 Compliance

Aids in achieving compliance with FDA regulations.

Tracking and Database

Provides a robust system for tracking trial information and metrics.

Automation and Consistency

Automates tasks and ensures consistency across trials.

Wide Range of Reporting Options

Offers various reporting capabilities.

Metric Measurements

Tracks and measures key performance indicators.

Investigator Payments

Manages investigator payments.

Site Contract and Payment Management

Handles site contracts and payments.

Real-time Site Portal

Provides sites with real-time access to relevant information.

Time & Expense Reporting

Tracks time and expenses associated with trials.

CTMS/EDC/IVRS Integration

Integrates with EDC and IVRS systems via Web Services or export/import.

On-line and Off-line Use

Allows for both online and offline access.

Hosted and/or Licensed Use

Offers flexible deployment options.

Email Alerts

Provides email alerts for important events.

Industry Standard Security

Incorporates security measures to protect data.

Templates

Offers templates for ease of use and efficiency.

Business Development Module

Includes a module for business development activities.

Pricing

Free trial
Free version
Request a quote
Promo Offer

Countries & Languages

Global
Countries served
7
Interface languages
10
Billing currencies

Interface languages

EnglishSpanishFrenchGermanItalianJapaneseChinese

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇨🇦CAD🇦🇺AUD🇯🇵JPY🇨🇭CHF🇨🇳CNY🇮🇳INR🇷🇺RUB

No reviews yet

Be the first to drop a review

Alternatives to Protocol Manager

Trium CTG Online logo

Trium CTG Online

Trium CTG Online is a web-based software platform from Trium Analysis Online GmbH that provides…

GRADEpro logo

GRADEpro

GRADEpro is a software platform designed to support evidence synthesis, clinical guideline development, and healthcare…

Z

Zapclinica

Zapclinica is a telemedicine and decentralized clinical trials platform from Zap Solutions that helps facilitate…

Verial eTMF logo

Verial eTMF

Verial eTMF is a clinical trial management software from Triall that delivers integrated technology and…

Veeva Vault Clinical Operations Suite logo

Veeva Vault Clinical Operations Suite

Veeva Vault Clinical Operations Suite is a cloud-based platform from Veeva that supports clinical trial…

Trials.ai logo

Trials.ai

Trials.ai is a clinical trial software platform from ZS that supports efficient trial design and…

Spot something wrong or outdated?

Suggest a correction — a reviewer verifies every change.

Often compared with Protocol Manager

Compare any two tools →
Trium CTG Online logo
Trium CTG Online
Remote Patient Monitoring
0.0
GRADEpro logo
GRADEpro
Clinical Trial Management
0.0
Z
Zapclinica
Clinical Trial Management
0.0
Verial eTMF logo
Verial eTMF
Clinical Trial Management
0.0