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What is Supply Chain Wizard Digital Factory?

Digital Logbook: Optimizing Room Logs for GMP Adherence. In the realm of pharmaceuticals, meticulous documentation of all processes in logbooks is critical to comply with Good Manufacturing Practice (GMP) guidelines. Conventional practices, including handwritten records or Excel sheets, can obstruct effective data analysis and escalate costs due to their labor-intensive upkeep and potential security vulnerabilities. Our innovative solution offers a straightforward, flexible, and expandable framework that facilitates the digitization of all room logs and forms, efficiently recording activities on the production floor. Users benefit from the convenience of secure data access anytime, anywhere, while the integration of personal digital signatures bolsters both security and quality. Our platform guarantees GMP compliance by generating immutable records and offers optional blockchain technology for enhanced protection. The user experience is streamlined, enabling line operators to log tasks or activities effortlessly with just a few clicks or taps, all while multiple security layers fortify the logbook's integrity. Additionally, tailored workflows accommodate your unique data entry and template approval needs, simplifying the process of maintaining compliance and operational efficiency. This contemporary method not only enhances record-keeping but also cultivates a strong sense of accountability within pharmaceutical operations, ultimately contributing to improved overall performance. As a result, organizations can focus more on their core activities, fostering innovation and excellence in the industry.

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

Supply Chain Wizard

Date Founded

2014

Company Location

United States

Company Website

solutions.supplychainwizard.com

Company Facts

Organization Name

Novatek International

Date Founded

1996

Company Location

Canada

Company Website

www.ntint.com

Categories and Features

Logbook

Asset Tracking
Audit Trails
Data Search
Employee Time Clock
For Drivers
For Pilots
User Access Permissions
Violation Tracking

OEE

Benchmarking
Cost Tracking
Downtime Tracking
Historical Reporting
Performance Metrics
Quality Control
Real Time Reporting
Root Cause Analysis
Trend Analysis
Work Order Management

Production Scheduling

"What If" Scenarios
Automated Scheduling
Bottleneck Optimization
Capacity Planning
Constraint Scheduling
Job Scheduling
Material Planning
Priority-Based Scheduling
Quality Control

Time Clock

Biometric Recognition
Hourly Employee Tracking
Messaging
Mobile Access
Online Punch Card
Payroll Management
Punch card
Reporting/Analytics
Salaried Employee Tracking
Sick Leave Tracking
Vacation / Leave Tracking
Workstation Tracking

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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