Nukleus logo

Nukleus

by nuvoteQ · Since 2015
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Active1+ countriesCloud
Quick facts
VendornuvoteQ
Year launched2015
StatusActive
LocationHazelwood Incub8tor, 47 Hazelwood Rd, Hazelwood, Pretoria, 0081, South Africa
Countries served1+
Languages1
Integrations
Free tier
Free trial
Contact salesYES

About Nukleus

Nukleus is a data integration software from nuvoteQ that provides a platform for managing and analyzing data across various sources. It combines data ingestion, change, and visualization capabilities so users can gain insights from their data effectively. Nukleus supports integration with multiple data sources, flexible data modeling, and real-time analytics to meet the diverse needs of organizations. The software is designed for scalability, ensuring it can handle growing data volumes as businesses expand. Key capabilities: data ingestion change tools visualization options real-time analytics integration with third-party applications Best for: data analysts and business intelligence professionals that need to unify and analyze data from multiple sources.

Nukleus by nuvoteQ is an impressive and comprehensive clinical research platform that addresses many of the inefficiencies inherent in traditional clinical trial management. Designed as a flexible electronic data capture system, it allows research teams to collect, manage, and analyse clinical data with a level of accuracy and speed that paper based systems cannot match. One of its standout features is the ability to function simultaneously as an eSource, EDC, and patient support program, meaning it can handle data from initial capture all the way through reporting and analysis, reducing the risk of errors and delays. The platform includes a smart visit scheduler that tracks participant timelines and highlights missed or overdue visits, ensuring studies remain on schedule. Integrated medical coding libraries like MedDRA and WHO‑DD ICD‑10 enable precise classification of medical events, while interactive response services facilitate randomisation and treatment allocation seamlessly. Its electronic patient reported outcomes tools, combined with configurable local lab modules that flag out‑of‑range results, make data monitoring more efficient and accurate.

Pros & Cons

What users like
  • +Eliminates manual, paper‑based data collection to speed up clinical trial workflows.
  • +Provides advanced scheduling and data quality checks that improve trial accuracy.
  • +Supports both patient input and laboratory integration for comprehensive data capture.
  • +Low‑code configuration reduces dependency on technical resources.
  • +Custom dashboards and reporting tools support diverse stakeholder needs.
What users flag
  • Requires training so users can fully leverage configurability and clinical features.
  • Effectiveness depends on reliable internet access and data quality from sites.
  • As a specialised clinical platform, it may be more complex than basic data tools.
  • Full value may require integration with other clinical systems and workflows.
  • Adoption costs can include setup, configuration, and training time.

Features

Key features

Electronic Data Capture (EDC)
Captures clinical trial data electronically to replace paper‑based methods and improve efficiency.
Visit Scheduler Wizard
Automates visit scheduling based on protocol timelines and flags overdue or missed visits.
Integrated Medical Coding
Supports standard coding libraries for accurate classification of medications and medical history.
Interactive Web Response Services
Handles tasks like randomisation, stratification, and real‑time allocation within trials.
Electronic Patient Reported Outcomes (ePRO)
Enables patients to submit questionnaire responses digitally.
Local Lab Module
Defines site‑specific lab reference ranges and matches data with checks during entry.
Low‑Code / No‑Code Configurability
Lets users configure workflows, logic, and dashboards without writing code.

Additional features

Customisable Dashboards
Allows personalised views of study data with configurable widgets.
Rapid Configuration Tools
Helps administrators set up studies quickly using intuitive front‑end tools.
Coding Libraries Support
Includes configurable medical coding standards for accuracy.
eSource Integration
Links with source data capture systems to reduce transcription and verification burden.
Report Builder
Enables stakeholders to generate reports tailored to their role and needs.
Audit Trail and Compliance
Tracks data changes and adheres to regulatory standards.
Role‑Based Access Controls
Supports secure access and permissions for different user types.

Pricing

Free trial
Free version
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Countries & Languages

1
Countries served
1
Interface languages
1
Billing currencies

Available in

Africa

Interface languages

English

Billing currencies

RAN

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