Audience

Life Sciences organizations, such as Biotech, Pharma, CRO, CMO/CDMO, Logistics, Labs, and more

About ZenQMS

ZenQMS is an AI-enabled electronic Quality Management System (eQMS) built for life sciences and GxP-regulated organizations, including biotech, pharma, CROs, and CMO/CDMO companies. The cloud-based, fully validated platform supports document control, training management, audits, supplier management, CAPA management, quality data intelligence, and compliance with FDA 21 CFR Part 11 and ISO standards.

Unlike legacy systems, ZenQMS is designed for companies of all sizes to be easier to use, quicker to validate, and more effective at managing GxP activities. ZenQMS supports key quality processes, including:

Document management/document control
Training management and learning management
CAPAs (Corrective and Preventive Actions)
Deviations, nonconformances, complaints, issues, and other quality events
Change controls
Audit management
Supplier and vendor management
Electronic signatures with 21 CFR Part 11-compliance
Risk management
Quality metrics tracking and reporting

Pricing

Pricing Details:
ZenQMS does not charge per seat license, allowing you to grow without sacrificing compliance. Our pricing is simple and transparent, and is based on the complexity of the account and initial migration/configuration activity. Contact ZenQMS today for more details.

Integrations

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Company Information

ZenQMS
Founded: 2010
United States
www.zenqms.com

Videos and Screen Captures

ZenQMS-AuditDetail

ZenQMS-AuditDetail

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Product Details

Platforms Supported
Cloud
Training
Documentation
Live Online
Webinars
In Person
Videos
Support
Phone Support
Online

ZenQMS Frequently Asked Questions

Q: What kinds of users and organization types does ZenQMS work with?
Q: What languages does ZenQMS support in their product?
Q: What kind of support options does ZenQMS offer?
Q: What other applications or services does ZenQMS integrate with?
Q: What type of training does ZenQMS provide?

ZenQMS Product 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