Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
QFacts is a comprehensive cloud-based Quality Management System designed specifically for pharmacies, compounding facilities, and other regulated sectors. It encompasses the entire quality lifecycle, featuring controlled document management with versioning and approval workflows, training and competency tracking with curriculum-aligned assignments, as well as event and complaint management, root cause analysis, CAPA oversight, and change control, all accompanied by thorough audit trails. This system is built to comply with GAMP 5 and adhere to European GMP and GDP standards, employing role-based access controls that span organizations, locations, and departments. Quality managers can customize review workflows, keep track of due dates, and oversee compliance via real-time dashboards. Each action taken within the system is meticulously logged and traceable, providing inspectors and auditors with a transparent chain of accountability that extends from document approval through to the completion of training and the resolution of corrective actions. By ensuring such detailed oversight, QFacts significantly enhances the overall efficiency and reliability of quality management processes.
Description
Managing Quality, Safety, and Environmental Management Systems may appear daunting and challenging to sustain. However, we are here to assist you, as we possess an in-depth understanding of the standards and have developed Toolbox to streamline your systems, ensure compliance, and enhance your business performance in the process. We firmly maintain that with the right approach, QHSE management systems can be straightforward and manageable; since they are grounded in robust business principles, implementing them leads to overall business improvement as well. This system serves as an organized workflow to manage, share, and oversee an organization’s files and documents effectively. By controlling your documents, you can save time, reduce effort and frustration, and minimize the risk to business continuity. The Toolkit features a workflow that accommodates both a version of a document that is still in development and a finalized version available for public access. Additionally, it retains previous versions and maintains a comprehensive audit log to track all changes. Team members have the ability to subscribe for updates, ensuring they stay informed about all modifications. Furthermore, this proactive approach not only simplifies document management but also fosters collaboration and transparency within the organization.
API Access
Has API
No
API Access
Has API
No
Screenshots View All
No images available
Integrations
No details available.
Integrations
No details available.
Pricing Details
$17/month/user
Free Trial
Yes
Free Version
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
No
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
Yes
In Person
No
Types of Training
Training Docs
No
Webinars
No
Live Training (Online)
Yes
In Person
No
Vendor Details
Company Name
QFacts
Founded
2024
Country
Belgium
Website
qfacts.be
Vendor Details
Company Name
Quality Systems Toolbox
Website
www.qualitysystems.com
Product Features
Quality Management
Audit Management
No
Complaint Management
No
Compliance Management
No
Corrective and Preventive Actions (CAPA)
No
Defect Tracking
No
Document Control
No
Equipment Management
No
ISO Standards Management
No
Maintenance Management
No
Risk Management
No
Supplier Quality Control
No
Training Management
No
Product Features
Quality Management
Audit Management
No
Complaint Management
Yes
Compliance Management
Yes
Corrective and Preventive Actions (CAPA)
Yes
Defect Tracking
No
Document Control
Yes
Equipment Management
Yes
ISO Standards Management
Yes
Maintenance Management
No
Risk Management
No
Supplier Quality Control
No
Training Management
No