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Clinical Trial Management Software

Clinical Assay Management Software

Software for managing clinical research study data and documents with one verified version of each data set

  • Workflow Management
  • Scheduling
  • 21 CFR Part 11 Compliance
  • Document Management
  • +12 more
Clinical Assay Management Software cover

About Clinical Assay Management Software

One record for each clinical data set

Novatek International's Clinical Assay Management Software gives one method for collecting, managing and protecting data from research trials. It is designed to hold the analytical data that supports a study alongside the clinical records. Every item of data is tracked as it is generated, and the software keeps one verifiable version of each clinical and analytical data set.

Documents and data integrity

A full documentation management function is included, so study documents sit alongside the data they describe. The company says the system is built around data integrity, meaning every item generated is tracked and users work from one verifiable version rather than competing copies.

A suite that connects with other quality tools

Novatek International describes itself as a provider of process-driven LIMS and other software for pharmaceutical, biotech and healthcare organizations. Clinical Assay sits in a wider suite that includes laboratory information management, stability management, environmental monitoring, water and utility monitoring, cleaning validation, quality management, calibration and preventive maintenance. The company's site says the products can be used on their own or connected together, and describes the suite as built for regulated operations, and that it has delivered quality software to regulated pharmaceutical operations since 1996. It also offers deployment, training, integration and validation documentation support.

TrustList summary

Clinical Assay Management Software is a Novatek International system for handling the data produced by clinical research studies. It is meant to give one consistent method for collecting, managing and protecting that data.

Main features

  • Data collection and management: a single approach to all clinical research study data.
  • Document management: a full documentation management function is included.
  • Data integrity: tracks all generated data and keeps a single verifiable version of every clinical and analytical data set.

Who it works with

Pharmaceutical, biotech and other healthcare organisations running clinical research.

Key facts

  • Vendor: Novatek International
  • Part of: a wider suite that includes LIMS, stability, environmental monitoring and quality management software

Summary written by TrustList from the business's own published information, Nov 2026.

Categories & features

  • Workflow Management
  • Scheduling
  • 21 CFR Part 11 Compliance
  • Document Management
  • Double Data Entry
  • Patient Monitoring
  • Installed - Mac
  • Installed - Windows
  • Web-Based, Cloud, SaaS
  • In Person
  • Live Online
  • Webinars
  • Documentation
  • Business Hours
  • Online
  • 24/7 (Live Rep)

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