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What is ZipQuality?

ZipQuality delivers a software-centric service aimed at assisting medical device manufacturers in the successful launch of pioneering products. Our collaborative platform skillfully handles rapid design changes for agile teams while ensuring compliance with regulatory requirements. Featuring a pre-configured system that integrates essential processes and tools, there's no need for alterations to your established quality system. The unified platform effectively supports quick design revisions for product documentation, maintaining consistency throughout. Our experienced consultants provide guidance to your team at every stage of the journey. Built upon the powerful ENOVIA platform, our extensive and scalable software solutions are customized to cater to your specific needs. This integrated approach enables swift design modifications while guaranteeing that product documentation and data are kept in sync, ensuring that all records are audit-ready. We address critical aspects such as product specifications, hardware, and software requirements, with a deep understanding of the challenges posed by software-intensive medical devices. The ZipQuality framework is designed around a methodical documentation strategy that strengthens systems engineering, fosters robust risk management, and guarantees clear traceability, thus becoming an essential tool for any medical device enterprise. Furthermore, our dedication to continuous enhancement ensures that we consistently refine our service offerings to stay in line with the latest developments in the industry, providing added value to our clients. In this ever-evolving landscape, having a partner like ZipQuality is crucial for maintaining a competitive edge.

What is Greenlight Guru?

Greenlight Guru serves more than 1,000 device manufacturers with a quality management system engineered specifically for medtech. Rather than forcing your workflow into a generic platform, the system is architected around regulatory reality. FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, EU MDR, and 21 CFR Part 11 compliance is aligned at the core, not added as an afterthought. Go live in weeks instead of quarters. You get 80+ pre-validated templates and medtech expert guidance, so you skip the separate validation project entirely. Greenlight Guru integrates AI automation to reduce manual work while maintaining the audit trail and documentation rigor your business demands. With 15 years specializing in medical device QMS, Greenlight Guru helps you pass inspections, accelerate time-to-market, and build lasting commercial success.

Media

Media

Integrations Supported

Integrations Supported

GitHub
Google Drive
Jira
Microsoft 365

API Availability

API Availability

Pricing Information

Pricing not provided

Pricing Information

Modules:
Document Management
Change Management
Training Management
Supplier Management
Design Controls
Risk Management
Parts Management
Quality Events
Software Parts
Software Release Management
SBOM Management
Software Test Automations

Pricing is custom scoped.

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Standard Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Not specified

Training Options

Documentation Hub
Webinars
Online Training

Company Facts

Organization Name

Consensia

Company Location

United States

Company Website

consensiainc.com/zipquality/

Company Facts

Organization Name

Greenlight Guru

Date Founded

2013

Company Location

United States

Company Website

greenlight.guru

Categories and Features

Quality Management

Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Document Control
Equipment Management
Risk Management

Categories and Features

Quality Management

Audit Management
Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Document Control
ISO Standards Management
Risk Management
Supplier Quality Control
Training Management

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