Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
Compliance Builder™, a real-time monitoring tool, is designed to enable 21 CFR Part 11 compliance. It provides data integrity across IT systems such file systems, laboratory and manufacturing instruments, as well as providing file system, database, laboratory, and manufacturing instrument data integrity. Compliance Builder allows you secure track all IT subsystems, including file systems, databases and laboratory equipment. It can be set up to monitor any file-based system, including file modifications and additions.
Description
Qualis LIMS is an enterprise-grade laboratory information management system that is widely used in various industry verticals, such as pharmaceuticals, life sciences, contract research, clinical research, and analytical and commercial sample testing.
This system has integrated modules designed to manage all laboratory processes, enabling labs to perform their tasks in an automated and paperless manner while ensuring compliance with regulatory requirements and industry standards.
Qualis LIMS is a digital transformation tool for laboratories, providing the following features:
• Efficient management, storage, and aliquoting of samples.
• Record keeping of test and experiment results, along with the management of tests, projects, samples, instruments, and inventory in a secure central database.
• Compliance with data integrity and regulatory requirements such as GxP, ISO17025, 21 CFR Part 11, and EudraLex Annex 11 without compromising quality.
API Access
Has API
No
API Access
Has API
No
Pricing Details
25000.00
Per user and server-based pricing
Free Trial
Yes
Free Version
No
Pricing Details
No price information available.
Free Trial
Yes
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
Yes
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
Yes
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
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
Yes
Live Training (Online)
Yes
In Person
Yes
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
No
Vendor Details
Company Name
Xybion
Founded
1977
Country
United States
Website
www.xybion.com/risk-compliance/cqrm-xd/compliance-builder/
Vendor Details
Company Name
Agaram Technologies
Founded
1998
Country
Chennai, India
Website
www.agaramtech.com/product/qualis-lims/
Product Features
Compliance
Archiving & Retention
No
Artificial Intelligence (AI)
No
Audit Management
Yes
Compliance Tracking
Yes
Controls Testing
No
Environmental Compliance
No
FDA Compliance
Yes
HIPAA Compliance
No
ISO Compliance
No
Incident Management
No
OSHA Compliance
No
Risk Management
Yes
Sarbanes-Oxley Compliance
Yes
Surveys & Feedback
No
Version Control
Yes
Workflow / Process Automation
No
Data Governance
Access Control
Yes
Data Discovery
No
Data Mapping
No
Data Profiling
No
Deletion Management
No
Email Management
No
Policy Management
No
Process Management
Yes
Roles Management
No
Storage Management
No
Database Monitoring
Anomaly Detection
No
Autodiscovery
No
Capacity Planning
No
Dashboard
Yes
Dependency Tracking
No
Historical Trend Analysis
No
Multitenancy
No
Notifications / Alerts
Yes
Performance Monitoring
No
Permissions / Access Controls
Yes
Predictive Analytics
Yes
Prioritization
No
Query Analysis
No
Resource Optimization
No
Troubleshooting
No
Digital Signature
Audit Trail
Yes
Authentication
No
Auto Reminders
No
Customizable Templates
Yes
Document Analytics
No
Mobile Signature
No
Multi-Party Signing
No
Progress Tracking
No
Task Progress Tracking
No
LIMS
Audit Trail
No
Certificates of Analysis
No
Data Import / Export
No
Electronic Laboratory Notebook
No
Inventory Management
No
Lab Instrument Interface
No
Reporting & Statistics
No
Sample Tracking
No
Specification Management
No
Workflow Management
No
Quality Management
Audit Management
Yes
Complaint Management
No
Compliance Management
Yes
Corrective and Preventive Actions (CAPA)
No
Defect Tracking
No
Document Control
Yes
Equipment Management
No
ISO Standards Management
No
Maintenance Management
No
Risk Management
No
Supplier Quality Control
No
Training Management
No
Product Features
Lab Inventory Management
Barcode Scanning
No
Expiration Date Management
No
Purchasing
No
Reorder Management
No
Sample Management
No
Supply Management
No
Usage Tracking
No
Vendor Management
No
LIMS
Audit Trail
Yes
Certificates of Analysis
Yes
Data Import / Export
No
Electronic Laboratory Notebook
Yes
Inventory Management
Yes
Lab Instrument Interface
Yes
Reporting & Statistics
No
Sample Tracking
Yes
Specification Management
Yes
Workflow Management
Yes
Medical Lab
Audit Trail
Yes
Data Analysis Auditing
No
Data Security
No
EMR Interface
No
Fax Management
No
Lab Instrument Interface
Yes
Multi-Location Printing
No
Online Instrumentation
No
Physician Test Panels
No
Procedure-Based Billing
Yes
Sample Tracking
No