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What is Enzyme QMS?

Our Quality Management System (QMS) features extensive modules that address every stage of the product life cycle, from Design Control to Corrective and Preventive Actions (CAPA). We provide your entire team with training and stand ready to support you whenever you need assistance. Enzyme Consulting, LLC. focuses on customizing and executing your Quality System to align with your unique requirements. After you finish the onboarding process, our team remains available for ongoing conversations and to answer any questions you might have. Established by experienced industry experts who were dissatisfied with existing QMS solutions, Enzyme's system is specifically crafted for life science companies, emphasizing the distinct challenges associated with developing FDA-regulated software. With the backing of our dedicated consultants, you can confidently bring your product to market. Our consultants not only have direct experience in the medical device industry but also excel in accurately assessing risks, which enables them to deeply understand the challenges encountered during product development. This comprehensive support ensures that you are not navigating these complexities on your own, allowing for a more seamless journey to successful product launch. Furthermore, our commitment to your success means we are continuously evolving our services to better meet your needs.

What is CAPA Manager?

Streamline the detection and resolution of issues within your organization and supply chain through automation. This CAPA software application is highly regarded and has gained the trust of thousands of users across the globe. The CAPA Manager software enhances the corrective action process by automating the assignment, notification, investigation, and reporting of corrective actions. By doing so, it reduces the likelihood of errors throughout the entire CAPA process, from initiation to investigation and final closure. Furthermore, CAPA Manager complies with key quality management standards such as ISO 9001, AS9100, and TS 16949. It effectively tracks records related to root-cause analysis and corrective actions, while also offering pre-defined workflows that include approval checkpoints to ensure thorough oversight. This comprehensive approach not only boosts efficiency but also enhances overall quality management within organizations.

Media

Media

Integrations Supported

GitHub
Jenkins
Jira

Integrations Supported

GitHub
Jenkins
Jira

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

$12.49 per user/month
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

Enzyme

Date Founded

2016

Company Location

United States

Company Website

www.enzyme.com

Company Facts

Organization Name

Adaptive Business Management Systems

Date Founded

2009

Company Location

United Kingdom

Company Website

www.adaptivebms.com/CAPA-Software/

Categories and 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

Categories and Features

CAPA

Audit Management
CAPA Planning
Change Management
Complaint Management
Incident Management
Nonconformance Tracking
Quality Control
Risk Management
Root Cause Analysis
Training Management

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

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