SimplerQMS
3.0 out of 5 starsRatings and Reviews 0 Ratings
Ratings and Reviews 2 Ratings
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What is ValGenesis?
ValGenesis's VLMS provides a comprehensive suite of features designed to improve traditional validation techniques. This platform offers a holistic view of the validation lifecycle, supported by a powerful management system, and integrates effortlessly with existing infrastructures. By employing paperless validation software, it streamlines workflows, incorporates compliance guidelines into these workflows, and enables electronic signatures through quick routing and timely alerts. Users can instantly access metrics, dashboards, and reports, which simplifies the process of fulfilling audit and inspection requirements with minimal effort. This approach not only enhances efficiency but also guarantees adherence to standards, fostering uniformity in managing requirements, testing methodologies, and risk evaluation practices. Furthermore, VLMS assists teams in identifying areas for continuous improvement, ultimately aiming to elevate the overall quality of validation processes.
What is SimplerQMS?
SimplerQMS is a specialized electronic Quality Management System (eQMS) tailored specifically for organizations in the Life Sciences sector. Designed by industry experts, our eQMS ensures compliance with essential regulations such as FDA, ISO, and GxP by facilitating automated and audit-ready quality processes.
The platform effectively centralizes and automates fundamental quality workflows within a fully validated, cloud-based system, allowing clients to minimize manual tasks, decrease errors, and maintain consistently organized records that are always inspection-ready.
In contrast to standard QMS tools, SimplerQMS is pre-configured to meet the unique requirements of the Life Sciences industry, incorporating templates, workflows, and controls that align with FDA 21 CFR Part 11, 210/211, 820, EU Annex 11, ISO 13485:2016, and other relevant standards.
Furthermore, clients benefit from a reliable partnership that provides extensive regulatory and quality knowledge, which includes access to audit-proven insights, advice from compliance experts, ongoing system validation, user training, round-the-clock global support, seamless implementation and data migration, along with dedicated Customer Success Experts.
Our mission is to empower Life Science companies in efficiently managing quality and regulatory documentation, enabling organizations to thrive from initial growth stages to global operations while enhancing compliance, operational control, and fostering a robust quality culture. By leveraging our expertise, businesses can streamline their processes and ensure they meet the highest industry standards.
Integrations Supported
API Availability
API Availability
Has API
Pricing Information
Pricing not provided
Pricing Information
$17,500 / year
We offer subscription-based pricing with everything you need – integrated QMS modules, full implementation and onboarding, validation, user training, cloud hosting, QMS templates, data migration, and ongoing support. No hidden costs.
Free Trial Offered?
Supported Platforms
SaaS
Windows
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
Customer Service / Support
Standard Support
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Training Options
Online Training
On-Site Training
Training Options
Documentation Hub
Online Training
Company Facts
Organization Name
ValGenesis
Date Founded
2005
Company Location
United States
Company Website
www.valgenesis.com
Company Facts
Organization Name
SimplerQMS
Date Founded
2017
Company Location
Denmark
Company Website
www.simplerqms.com
Categories and Features
Medical Lab
Not specified
Medical Quality Management Systems
Not specified
Categories and Features
Audit
Alerts / Notifications
Audit Planning
Compliance Management
Dashboard
Forms Management
Issue Management
Mobile Access
Risk Assessment
Workflow Management
CAPA
Audit Management
CAPA Planning
Change Management
Complaint Management
Incident Management
Nonconformance Tracking
Quality Control
Risk Management
Training Management
Compliance
Archiving & Retention
Audit Management
FDA Compliance
HIPAA Compliance
ISO Compliance
Risk Management
Version Control
Workflow / Process Automation
Document Control
Archiving & Retention
Automated Routing
Change Management
Compliance Management
Electronic Signature
Escalation Management
Periodic Review
Version Control
Electronic Batch Records (EBR)
Not specified
ISO Compliance
Not specified
Medical Quality Management Systems
Not specified
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