ResearchManager logo

ResearchManager

by Cloud9-Software · Since 2013
No reviews yet
ActiveAvailable globallyCloud
Quick facts
VendorCloud9-Software
Year launched2013
StatusActive
Location401 Park Avenue South, 10th Floor New York, 10016, USA
Countries servedGlobal
Languages3
Integrations10+
Free tier
Free trial
Contact salesYES

About ResearchManager

ResearchManager is a clinical research suite from Cloud9-Software that supports clinical data management in compliance with ISO 27001 and NEN 7510 standards. It provides clinical operations, research data analytics, and features such as ResearchManager Summit to help researchers manage their projects efficiently. The platform ensures adherence to GCP and GDPR regulations, making it suitable for handling sensitive data. Organizations can use the suite's capabilities to improve data integration, monitor trial progress, and identify trends in clinical research outcomes. Key capabilities: Clinical Data Management Clinical Operations ResearchManager Summit Best for: clinical research organizations that need a reliable platform for managing clinical trials and research projects.

ResearchManager is a comprehensive, cloud-based software suite designed to streamline clinical research processes. The Clinical Research Suite offers a wide range of tools that facilitate scalable and flexible solutions throughout the research journey. The platform focuses on enhancing efficiency in clinical data management, clinical operations, and compliance, all while reducing turnaround times and improving transparency. With its modern, customer-focused approach, ResearchManager enables researchers to manage their trials and data securely and in compliance with the latest regulations. The user interface of ResearchManager is designed to be intuitive and user-friendly, making it accessible to users across various roles within the research process. From clinical researchers to regulatory authorities, the system’s streamlined navigation ensures that all users can easily interact with the platform. The cloud-based nature of the software allows for seamless access across multiple devices and web browsers, ensuring flexibility and accessibility for users regardless of location. ResearchManager offers robust functionality through its various features, including Electronic Data Capture (EDC), Electronic Patient-Reported Outcomes (ePRO), Randomization and Trial Supply Management (RTSM), and Clinical Trial Management Systems (CTMS), among others.

Pros & Cons

What users like
  • +Significant improvement over previous software for research projects
  • +Great repository that streamlines the approval process
  • +Easy to use with good export options for trial data
  • +Saves time for staff and allows easy overviews for investigators and authorities
What users flag
  • Can be slow at times, which can be frustrating
  • No option to select multiple participants as 'missing'
  • Lacks some functionalities for easy navigation between sections
  • The document labeling system (letter + number) is annoying

Features

Key features

100% Compliance with Laws and Regulations
ResearchManager ensures that all tools comply with the latest clinical research regulations, offering a secure solution for data handling and compliance, making it suitable for any research project.
100% Customized Implementation
The platform allows for tailored solutions that meet the specific needs of each organization, ensuring that the system is customized to fit the user's requirements and workflows.
50% Faster Clinical Processes
ResearchManager accelerates clinical research operations by streamlining data handling, improving coordination, and reducing redundant tasks, ultimately speeding up the process by up to 50%.

Additional features

EDC (Electronic Data Capture)
A comprehensive tool for managing clinical data in a secure and compliant manner.
ePRO (Electronic Patient-Reported Outcomes)
Facilitates the collection of patient-reported outcomes electronically, improving data accuracy and patient engagement.
RTSM (Randomization and Trial Supply Management)
Manages trial supplies and randomization in clinical trials to ensure efficient allocation of resources.
Visit Planning
A tool that helps in planning and organizing clinical study visits, ensuring optimal scheduling.
eSource
Collects data directly from source documents and integrates it into the clinical trial system for streamlined data management.
eConsent
Digital consent management, allowing participants to provide consent electronically, improving the trial process and documentation.
CTMS (Clinical Trial Management System)
Manages clinical trial operations, such as trial timelines, subject tracking, and protocol compliance.
eTMF (Electronic Trial Master File)
Digitizes and stores trial master file documents, ensuring regulatory compliance and easy access to critical study documents.
RIMS (Regulatory Information Management System)
Helps in managing and tracking regulatory submissions and documentation.

Pricing

Free trial
Free version
Request a quote
Promo Offer

Countries & Languages

Global
Countries served
3
Interface languages
3
Billing currencies

Interface languages

DutchEnglishGerman

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP

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