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What is Predisys Analytical Suite?

Predisys focuses on delivering specialized solutions for quality assurance, test data oversight, and manufacturing intelligence, with the goal of enabling businesses to enhance product excellence, boost operational efficiency, reduce compliance expenditures, and improve transparency across the product lifecycle and supply chain. At the forefront of their offerings is the Predisys Analytical Suite, which features an array of tools tailored for gathering and managing quality and performance measurement data from diverse platforms, allowing for comprehensive analysis and reporting through sophisticated statistical process control (SPC) methodologies along with robust analytical and data visualization features. This software excels at transforming extensive amounts of inspection and testing information into actionable insights. Additionally, Predisys provides an enterprise-grade solution that is specifically designed to meet the unique requirements of the medical device, diagnostics, biotech, and pharmaceutical industries, ensuring adherence to FDA regulations while facilitating a cost-effective, flexible, and seamless shift from traditional paper documentation to a fully automated electronic management framework. Ultimately, Predisys is committed to optimizing workflows and improving decision-making for its clients, thereby promoting innovation and maintaining a competitive advantage in the marketplace. By leveraging their expertise, organizations can expect to see significant improvements in both operational effectiveness and product quality.

What is Nova-QMS?

Maintaining consistent product quality and effective quality management systems presents considerable obstacles in today's pharmaceutical manufacturing environment. Sectors subject to rigorous regulations, such as Pharmaceuticals, Biotechnology, and Life Sciences, are required to follow Good Manufacturing Practices (GMP) to meet legal requirements. However, simply meeting GMP standards is not sufficient; organizations must also demonstrate compliance through proper documentation. Utilizing paper-based forms, disconnected systems, or manual processes to manage, track, and document quality-related issues and their resolutions does not provide adequate solutions for creating cohesive and integrated quality management systems that meet industry expectations. As a result, it becomes imperative for organizations to adopt more sophisticated and automated solutions to bolster their quality assurance initiatives and facilitate smoother compliance processes, ultimately leading to improved operational efficiency and product safety.

Media

Media

Integrations Supported

Microsoft 365
Microsoft SharePoint

Integrations Supported

Microsoft 365
Microsoft SharePoint

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

Predisys

Company Website

www.predisys.com

Company Facts

Organization Name

Novatek International

Date Founded

1996

Company Location

Canada

Company Website

ntint.com/product/nova-qms/

Categories and Features

SPC

Corrective Actions (CAPA)
Data Entry
Data Linking
Data Management
Excel Loader
Job Management
OPC Data Collection
Performance Metrics
Point-of-Production Analysis
Real Time Data Collection
Regulatory Compliance

Categories and Features

Quality Management

Audit Management
Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Defect Tracking
Document Control
Equipment Management
ISO Standards Management
Maintenance Management
Risk Management
Supplier Quality Control
Training Management

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