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What is RQM+?

RQM+ is a leading global player in the medical technology service sector, focused on helping its clients achieve compliance and market success more quickly. Drawing from extensive knowledge and industry experience, we provide customized solutions that enhance the entire product lifecycle for medical technology companies, guiding them from the initial concept to commercialization and further. Our broad range of services ensures a smooth, end-to-end experience that touches every phase of medical device development. The quality assurance engineers at RQM+ carefully assess material lists, build supplier networks, and aid in managing the design change process. In a similar vein, our design quality engineers focus on critical components such as packaging integrity, sterility assurance, biocompatibility, and necessary device testing procedures. Our regulatory affairs consultants are essential in delivering expert guidance and support with submissions to the FDA, notified bodies, and other regulatory agencies, ensuring that our clients navigate compliance effectively. Furthermore, we utilize our extensive knowledge of current reimbursement protocols and value-based compensation systems to bolster our clients' market positions. By working closely with medical technology companies, RQM+ is devoted to supporting them in achieving their objectives both efficiently and effectively, thereby enhancing their overall market presence. Our mission is to create a lasting impact in the medical technology landscape through our dedicated services and strategic partnerships.

What is Orcanos ALM and QMS?

Orcanos provides a robust software solution designed for Application Lifecycle Management (ALM) and Quality Management Systems (QMS), ensuring that products are delivered on time and within budget. This efficient cloud-based platform integrates functionalities such as Requirements Management, Test Management, Document Control, Risk Management, and Quality Management into a single repository. Users benefit from intuitive dashboards and real-time alerts that enhance project monitoring and visibility throughout the development process. The Orcanos e-DMS serves as a comprehensive document management system, enabling users to create, track, search, archive, and approve documentation critical to each stage of medical device launch. By streamlining access to essential documents related to planning, design, development, manufacturing, and servicing, the e-DMS improves the efficiency of quality processes and significantly reduces time to market. Furthermore, this optimized workflow empowers organizations to prioritize innovation and adhere to regulatory standards while maintaining high levels of productivity, ultimately fostering a culture of continuous improvement.

Media

Media

Integrations Supported

Jira
Microsoft 365
Salesforce

Integrations Supported

Jira
Microsoft 365
Salesforce

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

$69.00/month/user
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

RQM+

Company Location

United States

Company Website

www.rqmplus.com

Company Facts

Organization Name

Orcanos

Date Founded

2004

Company Location

Israel

Company Website

www.orcanos.com/compliance/qpack-medical-compliance/

Categories and Features

Categories and Features

Application Lifecycle Management

Administrator Level Control
Defect Tracking
Iteration Planning
Project Management
Release Management
Requirements Review
Task Management
Test Case Tracking
User Level Management
Version Control

Requirements Management

Automated Functional Sizing
Automated Requirements QA
Automated Test Generation
Automated Use Case Modeling
Change Management
Collaboration
History Tracking
Prioritization
Reporting
Status Reporting
Status Tracking
Summary Reports
Task Management
To-Do List
Traceability
User Defined Attributes

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