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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.

What is GMPPro?

The pursuit of quality is an ongoing endeavor, necessitating a focused approach to sustain a competitive advantage in the modern business environment. In industries like pharmaceuticals, the success, regulatory endorsements, and acceptance are heavily reliant on upholding stringent quality benchmarks. The pharmaceutical sector is defined by strict regulations that complicate the management of business operations. To adeptly maneuver through this intricate landscape, it is crucial to consistently evaluate and enhance internal processes. Thus, implementing a comprehensive quality management system is essential. GMPPro, created by Motto Systems, stands out as a thorough and dependable quality management solution designed to tackle quality challenges encountered at every stage of drug development. This advanced platform encompasses the full range of production, quality control, quality assurance, and engineering, while also offering the flexibility of modular, standalone solutions. GMPPro is meticulously designed to provide complete oversight of operational processes and is backed by a team of seasoned industry experts, guaranteeing that quality remains a priority throughout pharmaceutical development. By utilizing such innovative systems, organizations can significantly improve their prospects for success in a rigorously regulated landscape, ultimately fostering trust and safety in the products they deliver. Adopting these advanced methodologies not only enhances compliance but also drives continuous improvement in operational excellence.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

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

Novatek International

Date Founded

1996

Company Location

Canada

Company Website

ntint.com/product/nova-qms/

Company Facts

Organization Name

Motto Systems

Date Founded

2013

Company Location

India

Company Website

www.mottosys.com/gmppro-suite.html

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

Categories and Features

Compliance

Archiving & Retention
Artificial Intelligence (AI)
Audit Management
Compliance Tracking
Controls Testing
Environmental Compliance
FDA Compliance
HIPAA Compliance
ISO Compliance
Incident Management
OSHA Compliance
Risk Management
Sarbanes-Oxley Compliance
Surveys & Feedback
Version Control
Workflow / Process Automation

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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