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What is POMS MES?

POMS places a strong emphasis on research and development for its manufacturing execution system (MES), leading to a highly adaptable and user-friendly solution that requires no customization. Impressively, none of our clients rely on bespoke solutions! Specifically tailored for the Life Sciences industry, POMSnet Aquila is a web-based MES that utilizes Microsoft .NET and HTML5 technologies. This entirely online platform features an intuitive interface that is simple to navigate and economical to implement and maintain. POMSnet Aquila provides a comprehensive array of features, including the management of recipes and specifications, oversight of materials, tracking of equipment, control of production orders, execution of recipes, electronic batch records, and device history. Additionally, POMSnet incorporates best practices and business logic specifically designed for Pharmaceutical Manufacturing Execution Systems, which helps ensure maximum operational efficiency and regulatory compliance. Continually updating its offerings allows POMS to adeptly respond to the evolving needs of the Life Sciences sector, reinforcing its position as a leader in the field. This commitment to innovation not only enhances user experience but also fosters long-term partnerships with clients.

What is Nova-Cleaning Validation?

Nova-Cleaning Validation software is essential for enhancing product integrity by adeptly handling changes and assessing the risks related to cross-contamination and impurities in a dynamic production environment. It diligently examines every modification concerning methods, APIs, products, equipment, and family groups to maintain product integrity while ensuring compliance with regulatory requirements. In addition, Nova-Cleaning Validation complies with the stipulations outlined in 21 CFR Part 11 and EU Annex 11, which further solidifies its reliability. The system utilizes a risk-based approach and is thoroughly designed in accordance with PDA Technical Reports 29 and 49, ISPE MaPP, and 21 CFR Part 211.67, positioning it as a trusted option for quality assurance in the pharmaceutical sector. This all-encompassing strategy not only protects product quality but also boosts the overall efficiency of the manufacturing process, ultimately leading to more reliable outcomes for stakeholders. By continuously adapting to new challenges in the industry, it ensures that the highest standards of quality are consistently met.

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

POMS

Company Website

www.poms.com

Company Facts

Organization Name

Novatek International

Date Founded

1996

Company Location

Canada

Company Website

www.ntint.com

Categories and Features

Manufacturing Execution

Document Management
Forecasting
Quality Control
Quote Management
Resource Management
Supplier Management
Supply Chain Management
Traceability

Categories and Features

Manufacturing

Accounting Integration
ERP
MES
MRP
Maintenance Management
Purchase Order Management
Quality Management
Quotes/Estimates
Reporting/Analytics
Safety Management
Shipping Management

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